메뉴 건너뛰기




Volumn 67, Issue 7, 2010, Pages 849-854

Mitochondrial respiratory chain dysfunction in muscle from patients with amyotrophic lateral sclerosis

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME C OXIDASE; MITOCHONDRIAL DNA;

EID: 77955036882     PISSN: 00039942     EISSN: 15383687     Source Type: Journal    
DOI: 10.1001/archneurol.2010.128     Document Type: Article
Times cited : (119)

References (51)
  • 1
    • 0036234975 scopus 로고    scopus 로고
    • Disease progression in amyotrophic lateral sclerosis: Predictors of survival
    • Magnus T, Beck M, Giess R, Puls I, Naumann M, Toyka KV. Disease progression in amyotrophic lateral sclerosis: predictors of survival. Muscle Nerve. 2002; 25(5):709-714.
    • (2002) Muscle Nerve , vol.25 , Issue.5 , pp. 709-714
    • Magnus, T.1    Beck, M.2    Giess, R.3    Puls, I.4    Naumann, M.5    Toyka, K.V.6
  • 2
    • 0027401203 scopus 로고
    • Mutation in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
    • Rosen DR, Siddique T, Patterson D, et al. Mutation in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. Nature. 1993; 362(6415):59-62.
    • (1993) Nature , vol.362 , Issue.6415 , pp. 59-62
    • Rosen, D.R.1    Siddique, T.2    Patterson, D.3
  • 4
    • 33744950956 scopus 로고    scopus 로고
    • Oxidative stress and antioxidant enzyme upregulation in SOD1-G93A mouse skeletal muscle
    • DOI 10.1002/mus.20542
    • Mahoney DJ, Kaczor JJ, Bourgeois J, Yasuda N, Tarnopolsky MA. Oxidative stress and antioxidant enzyme upregulation in SOD1-G93A mouse skeletal muscle. Muscle Nerve. 2006;33(6):809-816. (Pubitemid 43856799)
    • (2006) Muscle and Nerve , vol.33 , Issue.6 , pp. 809-816
    • Mahoney, D.J.1    Kaczor, J.J.2    Bourgeois, J.3    Yasuda, N.4    Tarnopolsky, M.A.5
  • 5
    • 2442658908 scopus 로고    scopus 로고
    • DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)
    • Chen YZ, Bennett CL, Huynh HM, et al. DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4). Am J Hum Genet. 2004; 74(6):1128-1135.
    • (2004) Am J Hum Genet , vol.74 , Issue.6 , pp. 1128-1135
    • Chen, Y.Z.1    Bennett, C.L.2    Huynh, H.M.3
  • 6
    • 0034785483 scopus 로고    scopus 로고
    • A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2
    • Hadano S, Hand CK, Osuga H, et al. A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2. Nat Genet. 2001;29 (2):166-173.
    • (2001) Nat Genet , vol.29 , Issue.2 , pp. 166-173
    • Hadano, S.1    Hand, C.K.2    Osuga, H.3
  • 7
    • 0034785509 scopus 로고    scopus 로고
    • The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis
    • Yang Y, Hentati A, Deng HX, et al. The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis. Nat Genet. 2001;29(2):160-165.
    • (2001) Nat Genet , vol.29 , Issue.2 , pp. 160-165
    • Yang, Y.1    Hentati, A.2    Deng, H.X.3
  • 8
    • 0037382240 scopus 로고    scopus 로고
    • Mutant dynactin in motor neuron disease
    • Puls I, Jonnakuty C, LaMonte BH, et al. Mutant dynactin in motor neuron disease. Nat Genet. 2003;33(4):455-456.
    • (2003) Nat Genet , vol.33 , Issue.4 , pp. 455-456
    • Puls, I.1    Jonnakuty, C.2    LaMonte, B.H.3
  • 9
    • 33645422711 scopus 로고    scopus 로고
    • ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis
    • Greenway MJ, Andersen PM, Russ C, et al. ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis. Nat Genet. 2006;38(4):411-413.
    • (2006) Nat Genet , vol.38 , Issue.4 , pp. 411-413
    • Greenway, M.J.1    Andersen, P.M.2    Russ, C.3
  • 11
    • 0036321382 scopus 로고    scopus 로고
    • Mitochondrial DNA and respiratory chain function in spinal cords of ALS patients
    • Wiedemann FR, Manfredi G, Mawrin C, Beal MF, Schon EA. Mitochondrial DNA and respiratory chain function in spinal cords of ALS patients. J Neurochem. 2002; 80(4):616-625.
    • (2002) J Neurochem , vol.80 , Issue.4 , pp. 616-625
    • Wiedemann, F.R.1    Manfredi, G.2    Mawrin, C.3    Beal, M.F.4    Schon, E.A.5
  • 12
    • 41949119043 scopus 로고    scopus 로고
    • TDP-43 A315T mutation in familial motor neuron disease
    • Gitcho MA, Baloh RH, Chakraverty S, et al. TDP-43 A315T mutation in familial motor neuron disease. Ann Neurol. 2008;63(4):535-538.
    • (2008) Ann Neurol , vol.63 , Issue.4 , pp. 535-538
    • Gitcho, M.A.1    Baloh, R.H.2    Chakraverty, S.3
  • 13
    • 63749096466 scopus 로고    scopus 로고
    • High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis
    • Corrado L, Ratti A, Gellera C, et al. High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis. Hum Mutat. 2009;30(4): 688-694.
    • (2009) Hum Mutat , vol.30 , Issue.4 , pp. 688-694
    • Corrado, L.1    Ratti, A.2    Gellera, C.3
  • 14
    • 41149180753 scopus 로고    scopus 로고
    • TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
    • Sreedharan J, Blair IP, Tripathi VB, et al. TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science. 2008;319(5870):1668-1672.
    • (2008) Science , vol.319 , Issue.5870 , pp. 1668-1672
    • Sreedharan, J.1    Blair, I.P.2    Tripathi, V.B.3
  • 15
    • 61349156118 scopus 로고    scopus 로고
    • Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis
    • Kwiatkowski TJ Jr, Bosco DA, LeClerc AL, et al. Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. Science. 2009; 323(5918):1205-1208.
    • (2009) Science , vol.323 , Issue.5918 , pp. 1205-1208
    • Kwiatkowski Jr., T.J.1    Bosco, D.A.2    LeClerc, A.L.3
  • 16
    • 61349162349 scopus 로고    scopus 로고
    • Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
    • Vance C, Rogelj B, Hortobágyi T, et al. Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. Science. 2009; 323(5918):1208-1211.
    • (2009) Science , vol.323 , Issue.5918 , pp. 1208-1211
    • Vance, C.1    Rogelj, B.2    Hortobágyi, T.3
  • 17
    • 0036156999 scopus 로고    scopus 로고
    • Amyotrophic Lateral Sclerosis. Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis
    • French ALS Research Group
    • Corcia P, Mayeux-Portas V, Khoris J, et al; French ALS Research Group. Amyotrophic Lateral Sclerosis. Abnormal SMN1 gene copy number is a susceptibility factor for amyotrophic lateral sclerosis. Ann Neurol. 2002;51(2):243-246.
    • (2002) Ann Neurol , vol.51 , Issue.2 , pp. 243-246
    • Corcia, P.1    Mayeux-Portas, V.2    Khoris, J.3
  • 20
    • 17844364182 scopus 로고    scopus 로고
    • Low levels of ALS-linked Cu/Zn superoxide dismutase increase the production of reactive oxygen species and cause mitochondrial damage and death in motor neuronlike cells
    • Rizzardini M, Mangolini A, Lupi M, Ubezio P, Bendotti C, Cantoni L. Low levels of ALS-linked Cu/Zn superoxide dismutase increase the production of reactive oxygen species and cause mitochondrial damage and death in motor neuronlike cells. J Neurol Sci. 2005;232(1-2):95-103.
    • (2005) J Neurol Sci , vol.232 , Issue.1-2 , pp. 95-103
    • Rizzardini, M.1    Mangolini, A.2    Lupi, M.3    Ubezio, P.4    Bendotti, C.5    Cantoni, L.6
  • 21
    • 0035886428 scopus 로고    scopus 로고
    • Early vacuolization and mitochondrial damage in motor neurons of FALS mice are not associated with apoptosis or with changes in cytochrome oxidase histochemical reactivity
    • DOI 10.1016/S0022-510X(01)00627-X, PII S0022510X0100627X
    • Bendotti C, Calvaresi N, Chiveri L, et al. Early vacuolation and mitochondrial damage in motor neurons of FALS mice are not associated with apoptosis or with changes in cytochrome oxidase histochemical reactivity. J Neurol Sci. 2001; 191(1-2):25-33. (Pubitemid 33035892)
    • (2001) Journal of the Neurological Sciences , vol.191 , Issue.1-2 , pp. 25-33
    • Bendotti, C.1    Calvaresi, N.2    Chiveri, L.3    Prelle, A.4    Moggio, M.5    Braga, M.6    Silani, V.7    De Biasi, S.8
  • 22
    • 0742321930 scopus 로고    scopus 로고
    • Oxidative stress: A common denominator in the pathogenesis of amyotrophic lateral sclerosis
    • Simpson EP, Yen AA, Appel SH. Oxidative stress: a common denominator in the pathogenesis of amyotrophic lateral sclerosis. Curr Opin Rheumatol. 2003; 15(6):730-736.
    • (2003) Curr Opin Rheumatol , vol.15 , Issue.6 , pp. 730-736
    • Simpson, E.P.1    Yen, A.A.2    Appel, S.H.3
  • 23
    • 32644434565 scopus 로고    scopus 로고
    • Is ALS a systemic disorder? Evidence from muscle mitochondria
    • Appel SH. Is ALS a systemic disorder? evidence from muscle mitochondria. Exp Neurol. 2006;198(1):1-3.
    • (2006) Exp Neurol , vol.198 , Issue.1 , pp. 1-3
    • Appel, S.H.1
  • 24
    • 65549128133 scopus 로고    scopus 로고
    • Muscle mitochondrial uncoupling dismantles neuromuscular junction and triggers distal degeneration of motor neurons
    • Dupuis L, Gonzalez de Aguilar JL, Echaniz-Laguna A, et al. Muscle mitochondrial uncoupling dismantles neuromuscular junction and triggers distal degeneration of motor neurons. PLoS One. 2009;4(4):e5390.
    • (2009) PLoS One , vol.4 , Issue.4
    • Dupuis, L.1    Gonzalez De Aguilar, J.L.2    Echaniz-Laguna, A.3
  • 25
    • 0036828796 scopus 로고    scopus 로고
    • Mitochondrial respiratory chain function in skeletal muscle of ALS patients
    • Echaniz-Laguna A, Zoll J, Ribera F, et al. Mitochondrial respiratory chain function in skeletal muscle of ALS patients. Ann Neurol. 2002;52(5):623-627.
    • (2002) Ann Neurol , vol.52 , Issue.5 , pp. 623-627
    • Echaniz-Laguna, A.1    Zoll, J.2    Ribera, F.3
  • 26
    • 23444445882 scopus 로고    scopus 로고
    • Mitochondrial changes in skeletal muscle in amyotrophic lateral sclerosis and other neurogenic atrophies
    • Krasnianski A, Deschauer M, Neudecker S, et al. Mitochondrial changes in skeletal muscle in amyotrophic lateral sclerosis and other neurogenic atrophies. Brain. 2005;128(pt 8):1870-1876.
    • (2005) Brain , vol.128 , Issue.PART 8 , pp. 1870-1876
    • Krasnianski, A.1    Deschauer, M.2    Neudecker, S.3
  • 27
    • 0030026832 scopus 로고    scopus 로고
    • Ultrastructural evidence for altered calcium in motor nerve terminals in amyotrophic lateral sclerosis
    • DOI 10.1002/ana.410390210
    • Siklós L, Engelhardt J, Harati Y, Smith RG, Joó F, Appel SH. Ultrastructural evidence for altered calcium in motor nerve terminals in amyotrophic lateral sclerosis. Ann Neurol. 1996;39(2):203-216. (Pubitemid 26071571)
    • (1996) Annals of Neurology , vol.39 , Issue.2 , pp. 203-216
    • Siklos, L.1    Engelhardt, J.2    Harati, Y.3    Smith, R.G.4    Joo, F.5    Appel, S.H.6
  • 28
    • 0942287085 scopus 로고    scopus 로고
    • Programmed cell death in amyotrophic lateral sclerosis: A mechanism of pathogenic and therapeutic importance
    • Przedborski S. Programmed cell death in amyotrophic lateral sclerosis: a mechanism of pathogenic and therapeutic importance. Neurologist. 2004;10(1):1-7.
    • (2004) Neurologist , vol.10 , Issue.1 , pp. 1-7
    • Przedborski, S.1
  • 29
    • 0019845220 scopus 로고
    • The ultrastructure of intramuscular nerves in amyotrophic lateral sclerosis
    • Atsumi T. The ultrastucture of intramuscular nerves in amyotrophic lateral sclerosis. Acta Neuropathol. 1981;55(3):193-198. (Pubitemid 12240160)
    • (1981) Acta Neuropathologica , vol.55 , Issue.3 , pp. 193-198
    • Atsumi, T.1
  • 30
    • 0030019414 scopus 로고    scopus 로고
    • Ultrastructural study of synapses in the anterior horn neurons of patients with amyotrophic lateral sclerosis
    • DOI 10.1016/0304-3940(96)12314-4
    • Sasaki S, Iwata M. Ultrastructural study of synapses in the anterior neurons of patients with amyotrophic lateral sclerosis. Neurosci Lett. 1996;204(1-2):53-56. (Pubitemid 26053674)
    • (1996) Neuroscience Letters , vol.204 , Issue.1-2 , pp. 53-56
    • Sasaki, S.1    Iwata, M.2
  • 31
    • 0013911740 scopus 로고
    • Ultrastructure of atrophic muscle in amyotrophic lateral sclerosis
    • Afifi AK, Aleu FP, Goodgold J, MacKay B. Ultrastructure of atrophic muscle in amyotrophic lateral sclerosis. Neurology. 1966;16(5):475-481.
    • (1966) Neurology , vol.16 , Issue.5 , pp. 475-481
    • Afifi, A.K.1    Aleu, F.P.2    Goodgold, J.3    MacKay, B.4
  • 32
    • 33846087291 scopus 로고    scopus 로고
    • Mitochondrial alterations in the spinal cord of patients with sporadic amyotrophic lateral sclerosis
    • DOI 10.1097/nen.0b013e31802c396b, PII 0000507220070100000002
    • Sasaki S, Iwata M. Mitochondrial alterations in the spinal cord of patients with sporadic amyotrophic lateral sclerosis. J Neuropathol Exp Neurol. 2007;66 (1):10-16. (Pubitemid 46066784)
    • (2007) Journal of Neuropathology and Experimental Neurology , vol.66 , Issue.1 , pp. 10-16
    • Sasaki, S.1    Iwata, M.2
  • 33
    • 0031915174 scopus 로고    scopus 로고
    • Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease
    • Comi GP, Bordoni A, Salani S, et al. Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease. Ann Neurol. 1998;43(1):110-116.
    • (1998) Ann Neurol , vol.43 , Issue.1 , pp. 110-116
    • Comi, G.P.1    Bordoni, A.2    Salani, S.3
  • 34
    • 40849130169 scopus 로고    scopus 로고
    • Amyotrophic lateral sclerosis with ragged red fibres
    • Hirano M, Angelini C, Montagna P, et al. Amyotrophic lateral sclerosis with ragged red fibres. Arch Neurol. 2008;65(3):403-406.
    • (2008) Arch Neurol , vol.65 , Issue.3 , pp. 403-406
    • Hirano, M.1    Angelini, C.2    Montagna, P.3
  • 35
    • 0028142392 scopus 로고
    • El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis: Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases and the El Escorial Clinical Limits of Amyotrophic Lateral Sclerosis workshop contributors
    • Brooks BR. El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis: Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases and the El Escorial Clinical Limits of Amyotrophic Lateral Sclerosis workshop contributors. J Neurol Sci. 1994;124(suppl):96-107.
    • (1994) J Neurol Sci , vol.124 , Issue.SUPPL. , pp. 96-107
    • Brooks, B.R.1
  • 37
    • 0034870693 scopus 로고    scopus 로고
    • Retrospective study of a large population of patients affected with mitochondrial disorders: Clinical, morphological and molecular genetic evaluation
    • Sciacco M, Prelle A, Comi GP, et al. Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluation. J Neurol. 2001;248(9):778-788.
    • (2001) J Neurol , vol.248 , Issue.9 , pp. 778-788
    • Sciacco, M.1    Prelle, A.2    Comi, G.P.3
  • 39
    • 0038446777 scopus 로고    scopus 로고
    • Sixteen novel mutations in the Cu/Zn superoxide dismutase gene in amyotrophic lateral sclerosis: A decade of discoveries, defects and disputes
    • Andersen PM, Sims KB, Xin WW, et al. Sixteen novel mutations in the Cu/Zn superoxide dismutase gene in amyotrophic lateral sclerosis: a decade of discoveries, defects and disputes. Amyotroph Lateral Scler Other Motor Neuron Disord. 2003;4(2):62-73.
    • (2003) Amyotroph Lateral Scler Other Motor Neuron Disord , vol.4 , Issue.2 , pp. 62-73
    • Andersen, P.M.1    Sims, K.B.2    Xin, W.W.3
  • 41
    • 58149234264 scopus 로고    scopus 로고
    • Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction
    • Corti S, Donadoni C, Ronchi D, et al. Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction. J Neurol Sci. 2009; 276(1-2):170-174.
    • (2009) J Neurol Sci , vol.276 , Issue.1-2 , pp. 170-174
    • Corti, S.1    Donadoni, C.2    Ronchi, D.3
  • 42
    • 0033556363 scopus 로고    scopus 로고
    • Spinal muscular atrophylike picture, cardiomyopathy and cytochrome c oxidase deficiency
    • Rubio-Gozalbo ME, Smeitink JA, Ruitenbeek W, et al. Spinal muscular atrophylike picture, cardiomyopathy and cytochrome c oxidase deficiency. Neurology. 1999;52(2):383-386.
    • (1999) Neurology , vol.52 , Issue.2 , pp. 383-386
    • Rubio-Gozalbo, M.E.1    Smeitink, J.A.2    Ruitenbeek, W.3
  • 43
    • 0037254203 scopus 로고    scopus 로고
    • Mitochondriopathy mimicking amyotrophic lateral sclerosis
    • Finsterer J. Mitochondriopathy mimicking amyotrophic lateral sclerosis. Neurologist. 2003;9(1):45-48.
    • (2003) Neurologist , vol.9 , Issue.1 , pp. 45-48
    • Finsterer, J.1
  • 44
    • 5144225349 scopus 로고    scopus 로고
    • Monomelic amyotrophy associated with the 7472insC mutation in the mtDNA tRNA ser(UCN) gene
    • Fetoni V, Briem E, Carrara F, Mora M, Zeviani M. Monomelic amyotrophy associated with the 7472insC mutation in the mtDNA tRNA ser(UCN) gene. Neuromuscul Disord. 2004;14(11):723-726.
    • (2004) Neuromuscul Disord , vol.14 , Issue.11 , pp. 723-726
    • Fetoni, V.1    Briem, E.2    Carrara, F.3    Mora, M.4    Zeviani, M.5
  • 45
    • 33644832850 scopus 로고    scopus 로고
    • Motoneuron disease in a patient with a mitochondrial tRNA ile mutation
    • Borthwick GM, Taylor RW, Walls TJ, et al. Motoneuron disease in a patient with a mitochondrial tRNA ile mutation. Ann Neurol. 2006;59(3):570-574.
    • (2006) Ann Neurol , vol.59 , Issue.3 , pp. 570-574
    • Borthwick, G.M.1    Taylor, R.W.2    Walls, T.J.3
  • 47
    • 55149119156 scopus 로고    scopus 로고
    • Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegia
    • Virgilio R, Ronchi D, Hadjigeorgiou GM, et al. Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegia. J Neurol. 2008; 255(9):1384-1391.
    • (2008) J Neurol , vol.255 , Issue.9 , pp. 1384-1391
    • Virgilio, R.1    Ronchi, D.2    Hadjigeorgiou, G.M.3
  • 48
    • 0033917463 scopus 로고    scopus 로고
    • Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis
    • Vielhaber S, Kunz D, Winkler K, et al. Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis. Brain. 2000; 123(pt 7):1339-1348.
    • (2000) Brain , vol.123 , Issue.PART 7 , pp. 1339-1348
    • Vielhaber, S.1    Kunz, D.2    Winkler, K.3
  • 49
    • 32644434546 scopus 로고    scopus 로고
    • Muscular mitochondrial function in amyotrophic lateral sclerosis is progressively altered as the disease develops: A temporal study in man
    • DOI 10.1016/j.expneurol.2005.07.020, PII S0014488605002694
    • Echaniz-Laguna A, Zoll J, Ponsot E, et al. Muscular mitochondrial function in amyotrophic lateral sclerosis is progressively altered as the disease develops: a temporal study in man. Exp Neurol. 2006;198(1):25-30. (Pubitemid 43243741)
    • (2006) Experimental Neurology , vol.198 , Issue.1 , pp. 25-30
    • Echaniz-Laguna, A.1    Zoll, J.2    Ponsot, E.3    N'Guessan, B.4    Tranchant, C.5    Loeffler, J.-P.6    Lampert, E.7
  • 50
    • 9844235346 scopus 로고    scopus 로고
    • Mitochondrial involvement in the ageing process: Facts and controversies
    • Brierley EJ, Johnson MA, James OFW, Turnbull DM. Mitochondrial involvement in the ageing process: facts and controversies. Mol Cell Biochem. 1997;174 (1-2):325-328.
    • (1997) Mol Cell Biochem , vol.174 , Issue.1-2 , pp. 325-328
    • Brierley, E.J.1    Johnson, M.A.2    James, O.F.W.3    Turnbull, D.M.4
  • 51
    • 0031885843 scopus 로고    scopus 로고
    • Role of mitochondrial DNA mutations in human aging: Implications for the central nervous system and muscle
    • Brierley EJ, Johnson MA, Lightowlers RN, James OF, Turnbull DM. Role of mitochondrial DNA mutations in human aging: implications for the central nervous system and muscle. Ann Neurol. 1998;43(2):217-223.
    • (1998) Ann Neurol , vol.43 , Issue.2 , pp. 217-223
    • Brierley, E.J.1    Johnson, M.A.2    Lightowlers, R.N.3    James, O.F.4    Turnbull, D.M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.