-
1
-
-
42749087763
-
The mitochondrial impairment, oxidative stress and neurodegeneration connection: Reality or just an attractive hypothesis?
-
PMID: 18403030
-
Fukui H, Moraes CT. The mitochondrial impairment, oxidative stress and neurodegeneration connection: reality or just an attractive hypothesis? Trends Neurosci 2008; 31:251-256. [PMID: 18403030]
-
(2008)
Trends Neurosci
, vol.31
, pp. 251-256
-
-
Fukui, H.1
Moraes, C.T.2
-
2
-
-
33750347347
-
Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases
-
PMID: 17051205
-
Lin MT, Beal MF. Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases. Nature 2006; 443:787-795. [PMID: 17051205]
-
(2006)
Nature
, vol.443
, pp. 787-795
-
-
Lin, M.T.1
Beal, M.F.2
-
3
-
-
0029045299
-
Mitochondrial DNA variation in human evolution, degenerative disease, and aging
-
PMID: 7668244
-
Wallace DC. Mitochondrial DNA variation in human evolution, degenerative disease, and aging. Am J Hum Genet 1995; 57:201-223. [PMID: 7668244]
-
(1995)
Am J Hum Genet
, vol.57
, pp. 201-223
-
-
Wallace, D.C.1
-
4
-
-
0037385480
-
Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease
-
PMID: 12618962
-
van der Walt JM, Nicodemus KK, Martin ER, Scott WK, Nance MA, Watts RL, Hubble JP, Haines JL, Koller WC, Lyons K, Pahwa R, Stern MB, Colcher A, Hiner BC, Jankovic J, Ondo WG, Allen FH Jr, Goetz CG, Small GW, Mastaglia F, Stajich JM, McLaurin AC, Middleton LT, Scott BL, Schmechel DE, Pericak-Vance MA, Vance JM. Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease. Am J Hum Genet 2003; 72:804-811. [PMID: 12618962]
-
(2003)
Am J Hum Genet
, vol.72
, pp. 804-811
-
-
van der Walt, J.M.1
Nicodemus, K.K.2
Martin, E.R.3
Scott, W.K.4
Nance, M.A.5
Watts, R.L.6
Hubble, J.P.7
Haines, J.L.8
Koller, W.C.9
Lyons, K.10
Pahwa, R.11
Stern, M.B.12
Colcher, A.13
Hiner, B.C.14
Jankovic, J.15
Ondo, W.G.16
Allen Jr., F.H.17
Goetz, C.G.18
Small, G.W.19
Mastaglia, F.20
Stajich, J.M.21
McLaurin, A.C.22
Middleton, L.T.23
Scott, B.L.24
Schmechel, D.E.25
Pericak-Vance, M.A.26
Vance, J.M.27
more..
-
5
-
-
67650976561
-
Mitochondrial haplogroups associated with Japanese centenarians, Alzheimer's patients, Parkinson's patients, type 2 diabetic patients and healthy non-obese young males
-
PMID: 19631917
-
Takasaki S. Mitochondrial haplogroups associated with Japanese centenarians, Alzheimer's patients, Parkinson's patients, type 2 diabetic patients and healthy non-obese young males. J Genet Genomics 2009; 36:425-434. [PMID: 19631917]
-
(2009)
J Genet Genomics
, vol.36
, pp. 425-434
-
-
Takasaki, S.1
-
6
-
-
20144389920
-
Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD
-
PMID: 15786469
-
Pyle A, Foltynie T, Tiangyou W, Lambert C, Keers SM, Allcock LM, Davison J, Lewis SJ, Perry RH, Barker R, Burn DJ, Chinnery PF. Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD. Ann Neurol 2005; 57:564-567. [PMID: 15786469]
-
(2005)
Ann Neurol
, vol.57
, pp. 564-567
-
-
Pyle, A.1
Foltynie, T.2
Tiangyou, W.3
Lambert, C.4
Keers, S.M.5
Allcock, L.M.6
Davison, J.7
Lewis, S.J.8
Perry, R.H.9
Barker, R.10
Burn, D.J.11
Chinnery, P.F.12
-
7
-
-
51449098994
-
Investigation of the role of mitochondrial DNA in multiple sclerosis susceptibility
-
PMID: 18682780
-
Ban M, Elson J, Walton A, Turnbull D, Compston A, Chinnery P, Sawcer S. Investigation of the role of mitochondrial DNA in multiple sclerosis susceptibility. PLoS One 2008; 3:e2891. [PMID: 18682780]
-
(2008)
PLoS One
, vol.3
-
-
Ban, M.1
Elson, J.2
Walton, A.3
Turnbull, D.4
Compston, A.5
Chinnery, P.6
Sawcer, S.7
-
8
-
-
33645014231
-
Does the mitochondrial genome play a role in the etiology of Alzheimer's disease?
-
PMID: 16408223
-
Elson JL, Herrnstadt C, Preston G, Thal L, Morris CM, Edwardson JA, Beal MF, Turnbull DM, Howell N. Does the mitochondrial genome play a role in the etiology of Alzheimer's disease? Hum Genet 2006; 119:241-254. [PMID: 16408223]
-
(2006)
Hum Genet
, vol.119
, pp. 241-254
-
-
Elson, J.L.1
Herrnstadt, C.2
Preston, G.3
Thal, L.4
Morris, C.M.5
Edwardson, J.A.6
Beal, M.F.7
Turnbull, D.M.8
Howell, N.9
-
9
-
-
34547796899
-
Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background
-
PMID: 17668373
-
Hudson G, Carelli V, Spruijt L, Gerards M, Mowbray C, Achilli A, Pyle A, Elson J, Howell N, La Morgia C, Valentino ML, Huoponen K, Savontaus ML, Nikoskelainen E, Sadun AA, Salomao SR, Belfort R Jr, Griffiths P, Man PY, de Coo RF, Horvath R, Zeviani M, Smeets HJ, Torroni A, Chinnery PF. Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background. Am J Hum Genet 2007; 81:228-233. [PMID: 17668373]
-
(2007)
Am J Hum Genet
, vol.81
, pp. 228-233
-
-
Hudson, G.1
Carelli, V.2
Spruijt, L.3
Gerards, M.4
Mowbray, C.5
Achilli, A.6
Pyle, A.7
Elson, J.8
Howell, N.9
la Morgia, C.10
Valentino, M.L.11
Huoponen, K.12
Savontaus, M.L.13
Nikoskelainen, E.14
Sadun, A.A.15
Salomao, S.R.16
Belfort Jr., R.17
Griffiths, P.18
Man, P.Y.19
de Coo, R.F.20
Horvath, R.21
Zeviani, M.22
Smeets, H.J.23
Torroni, A.24
Chinnery, P.F.25
more..
-
10
-
-
57049107326
-
Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of Leber hereditary optic neuropathy in Chinese families with the m. 11778G→A mutation
-
PMID: 19026397
-
Ji Y, Zhang AM, Jia X, Zhang YP, Xiao X, Li S, Guo X, Bandelt HJ, Zhang Q, Yao YG. Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of Leber hereditary optic neuropathy in Chinese families with the m. 11778G→A mutation. Am J Hum Genet 2008; 83:760-768. [PMID: 19026397]
-
(2008)
Am J Hum Genet
, vol.83
, pp. 760-768
-
-
Ji, Y.1
Zhang, A.M.2
Jia, X.3
Zhang, Y.P.4
Xiao, X.5
Li, S.6
Guo, X.7
Bandelt, H.J.8
Zhang, Q.9
Yao, Y.G.10
-
11
-
-
34548612004
-
Mitochondrial DNA haplogroups and age-related maculopathy
-
PMID: 17846364
-
Jones MM, Manwaring N, Wang JJ, Rochtchina E, Mitchell P, Sue CM. Mitochondrial DNA haplogroups and age-related maculopathy. Arch Ophthalmol 2007; 125:1235-1240. [PMID: 17846364]
-
(2007)
Arch Ophthalmol
, vol.125
, pp. 1235-1240
-
-
Jones, M.M.1
Manwaring, N.2
Wang, J.J.3
Rochtchina, E.4
Mitchell, P.5
Sue, C.M.6
-
12
-
-
66849130909
-
Mitochondrial DNA haplogroups associated with age-related macular degeneration
-
PMID: 19151382
-
Udar N, Atilano SR, Memarzadeh M, Boyer DS, Chwa M, Lu S, Maguen B, Langberg J, Coskun P, Wallace DC, Nesburn AB, Khatibi N, Hertzog D, Le K, Hwang D, Kenney MC. Mitochondrial DNA haplogroups associated with age-related macular degeneration. Invest Ophthalmol Vis Sci 2009; 50:2966-2974. [PMID: 19151382]
-
(2009)
Invest Ophthalmol Vis Sci
, vol.50
, pp. 2966-2974
-
-
Udar, N.1
Atilano, S.R.2
Memarzadeh, M.3
Boyer, D.S.4
Chwa, M.5
Lu, S.6
Maguen, B.7
Langberg, J.8
Coskun, P.9
Wallace, D.C.10
Nesburn, A.B.11
Khatibi, N.12
Hertzog, D.13
Le, K.14
Hwang, D.15
Kenney, M.C.16
-
13
-
-
0032904495
-
MtDNA haplogroup J: A contributing factor of optic neuritis
-
PMID: 10234520
-
Reynier P, Penisson-Besnier I, Moreau C, Savagner F, Vielle B, Emile J, Dubas F, Malthiery Y. mtDNA haplogroup J: a contributing factor of optic neuritis. Eur J Hum Genet 1999; 7:404-406. [PMID: 10234520]
-
(1999)
Eur J Hum Genet
, vol.7
, pp. 404-406
-
-
Reynier, P.1
Penisson-Besnier, I.2
Moreau, C.3
Savagner, F.4
Vielle, B.5
Emile, J.6
Dubas, F.7
Malthiery, Y.8
-
14
-
-
0030499127
-
Epidemiology of myopia
-
PMID: 9021311
-
Saw SM, Katz J, Schein OD, Chew SJ, Chan TK. Epidemiology of myopia. Epidemiol Rev 1996; 18:175-187. [PMID: 9021311]
-
(1996)
Epidemiol Rev
, vol.18
, pp. 175-187
-
-
Saw, S.M.1
Katz, J.2
Schein, O.D.3
Chew, S.J.4
Chan, T.K.5
-
15
-
-
55449092600
-
Identification and replication of three novel myopia common susceptibility gene loci on chromosome 3q26 using linkage and linkage disequilibrium mapping
-
PMID: 18846214
-
Andrew T, Maniatis N, Carbonaro F, Liew SH, Lau W, Spector TD, Hammond CJ. Identification and replication of three novel myopia common susceptibility gene loci on chromosome 3q26 using linkage and linkage disequilibrium mapping. PLoS Genet 2008; 4:e1000220. [PMID: 18846214]
-
(2008)
PLoS Genet
, vol.4
-
-
Andrew, T.1
Maniatis, N.2
Carbonaro, F.3
Liew, S.H.4
Lau, W.5
Spector, T.D.6
Hammond, C.J.7
-
16
-
-
33751418375
-
Identification of apolipoprotein A-I as a "STOP" signal for myopia
-
PMID: 16921168
-
Bertrand E, Fritsch C, Diether S, Lambrou G, Muller D, Schaeffel F, Schindler P, Schmid KL, van Oostrum J, Voshol H. Identification of apolipoprotein A-I as a "STOP" signal for myopia. Mol Cell Proteomics 2006; 5:2158-2166. [PMID: 16921168]
-
(2006)
Mol Cell Proteomics
, vol.5
, pp. 2158-2166
-
-
Bertrand, E.1
Fritsch, C.2
Diether, S.3
Lambrou, G.4
Muller, D.5
Schaeffel, F.6
Schindler, P.7
Schmid, K.L.8
van Oostrum, J.9
Voshol, H.10
-
17
-
-
0021675467
-
Nuclear cataract and myopia during hyperbaric oxygen therapy
-
PMID: 6691953
-
Palmquist BM, Philipson B, Barr PO. Nuclear cataract and myopia during hyperbaric oxygen therapy. Br J Ophthalmol 1984; 68:113-117. [PMID: 6691953]
-
(1984)
Br J Ophthalmol
, vol.68
, pp. 113-117
-
-
Palmquist, B.M.1
Philipson, B.2
Barr, P.O.3
-
18
-
-
0030199048
-
Myopia associated with hyperbaric oxygen therapy
-
PMID: 8843129
-
Ross ME, Yolton DP, Yolton RL, Hyde KD. Myopia associated with hyperbaric oxygen therapy. Optom Vis Sci 1996;73:487-494. [PMID: 8843129]
-
(1996)
Optom Vis Sci
, vol.73
, pp. 487-494
-
-
Ross, M.E.1
Yolton, D.P.2
Yolton, R.L.3
Hyde, K.D.4
-
19
-
-
4444292448
-
Ocular refractive changes in patients receiving hyperbaric oxygen administered by oronasal mask or hood
-
PMID: 15291940
-
Evanger K, Haugen OH, Irgens A, Aanderud L, Thorsen E. Ocular refractive changes in patients receiving hyperbaric oxygen administered by oronasal mask or hood. Acta Ophthalmol Scand 2004; 82:449-453. [PMID: 15291940]
-
(2004)
Acta Ophthalmol Scand
, vol.82
, pp. 449-453
-
-
Evanger, K.1
Haugen, O.H.2
Irgens, A.3
Aanderud, L.4
Thorsen, E.5
-
20
-
-
28444456056
-
Low levels of pigment epitheliumderived factor in highly myopic eyes with chorioretinal atrophy
-
PMID: 16310484
-
Ogata N, Imaizumi M, Miyashiro M, Arichi M, Matsuoka M, Ando A, Matsumura M. Low levels of pigment epitheliumderived factor in highly myopic eyes with chorioretinal atrophy. Am J Ophthalmol 2005; 140:937-939. [PMID: 16310484]
-
(2005)
Am J Ophthalmol
, vol.140
, pp. 937-939
-
-
Ogata, N.1
Imaizumi, M.2
Miyashiro, M.3
Arichi, M.4
Matsuoka, M.5
Ando, A.6
Matsumura, M.7
-
22
-
-
34347375054
-
Candidate gene and locus analysis of myopia
-
PMID: 17653045
-
Mutti DO, Cooper ME, O'Brien S, Jones LA, Marazita ML, Murray JC, Zadnik K. Candidate gene and locus analysis of myopia. Mol Vis 2007; 13:1012-1019. [PMID: 17653045]
-
(2007)
Mol Vis
, vol.13
, pp. 1012-1019
-
-
Mutti, D.O.1
Cooper, M.E.2
O'Brien, S.3
Jones, L.A.4
Marazita, M.L.5
Murray, J.C.6
Zadnik, K.7
-
23
-
-
26244468175
-
A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612
-
PMID: 16052171
-
Zhang Q, Guo X, Xiao X, Jia X, Li S, Hejtmancik JF. A new locus for autosomal dominant high myopia maps to 4q22-q27 between D4S1578 and D4S1612. Mol Vis 2005; 11:554-560. [PMID: 16052171]
-
(2005)
Mol Vis
, vol.11
, pp. 554-560
-
-
Zhang, Q.1
Guo, X.2
Xiao, X.3
Jia, X.4
Li, S.5
Hejtmancik, J.F.6
-
24
-
-
33745905223
-
Novel locus for X linked recessive high myopia maps to Xq23-q25 but outside MYP1
-
PMID: 16648373
-
Zhang Q, Guo X, Xiao X, Jia X, Li S, Hejtmancik JF. Novel locus for X linked recessive high myopia maps to Xq23-q25 but outside MYP1. J Med Genet 2006; 43:e20. [PMID: 16648373]
-
(2006)
J Med Genet
, vol.43
-
-
Zhang, Q.1
Guo, X.2
Xiao, X.3
Jia, X.4
Li, S.5
Hejtmancik, J.F.6
-
25
-
-
34247586191
-
Confirmation of a genetic locus for X-linked recessive high myopia outside MYP1
-
PMID: 17351708
-
Zhang Q, Li S, Xiao X, Jia X, Guo X. Confirmation of a genetic locus for X-linked recessive high myopia outside MYP1. J Hum Genet 2007; 52:469-472. [PMID: 17351708]
-
(2007)
J Hum Genet
, vol.52
, pp. 469-472
-
-
Zhang, Q.1
Li, S.2
Xiao, X.3
Jia, X.4
Guo, X.5
-
26
-
-
74749092186
-
Tracing the origins of Hakka and Chaoshanese by mitochondrial DNA analysis
-
PMID: 19591216
-
Wang WZ, Wang CY, Cheng YT, Xu AL, Zhu CL, Wu SF, Kong QP, Zhang YP. Tracing the origins of Hakka and Chaoshanese by mitochondrial DNA analysis. Am J Phys Anthropol 2010; 141:124-130. [PMID: 19591216]
-
(2010)
Am J Phys Anthropol
, vol.141
, pp. 124-130
-
-
Wang, W.Z.1
Wang, C.Y.2
Cheng, Y.T.3
Xu, A.L.4
Zhu, C.L.5
Wu, S.F.6
Kong, Q.P.7
Zhang, Y.P.8
-
27
-
-
0032868141
-
Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA
-
PMID: 10508508
-
Andrews RM, Kubacka I, Chinnery PF, Lightowlers RN, Turnbull DM, Howell N. Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA. Nat Genet 1999; 23:147. [PMID: 10508508]
-
(1999)
Nat Genet
, vol.23
, pp. 147
-
-
Andrews, R.M.1
Kubacka, I.2
Chinnery, P.F.3
Lightowlers, R.N.4
Turnbull, D.M.5
Howell, N.6
-
28
-
-
0036177751
-
Phylogeographic differentiation of mitochondrial DNA in Han Chinese
-
PMID: 11836649
-
Yao YG, Kong QP, Bandelt HJ, Kivisild T, Zhang YP. Phylogeographic differentiation of mitochondrial DNA in Han Chinese. Am J Hum Genet 2002; 70:635-651. [PMID: 11836649]
-
(2002)
Am J Hum Genet
, vol.70
, pp. 635-651
-
-
Yao, Y.G.1
Kong, Q.P.2
Bandelt, H.J.3
Kivisild, T.4
Zhang, Y.P.5
-
29
-
-
35448935610
-
Yao YG. mtDNA haplogroup distribution in Chinese patients with Leber's hereditary optic neuropathy and G11778A mutation
-
PMID: 17942074
-
Ji Y, Jia X, Zhang Q, Yao YG. mtDNA haplogroup distribution in Chinese patients with Leber's hereditary optic neuropathy and G11778A mutation. Biochem Biophys Res Commun 2007; 364:238-242. [PMID: 17942074]
-
(2007)
Biochem Biophys Res Commun
, vol.364
, pp. 238-242
-
-
Ji, Y.1
Jia, X.2
Zhang, Q.3
-
30
-
-
33745275886
-
Zhang YP. Updating the East Asian mtDNA phylogeny: A prerequisite for the identification of pathogenic mutations
-
PMID: 16714301
-
Kong QP, Bandelt HJ, Sun C, Yao YG, Salas A, Achilli A, Wang CY, Zhong L, Zhu CL, Wu SF, Torroni A, Zhang YP. Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations. Hum Mol Genet 2006; 15:2076-2086. [PMID: 16714301]
-
(2006)
Hum Mol Genet
, vol.15
, pp. 2076-2086
-
-
Kong, Q.P.1
Bandelt, H.J.2
Sun, C.3
Yao, Y.G.4
Salas, A.5
Achilli, A.6
Wang, C.Y.7
Zhong, L.8
Zhu, C.L.9
Wu, S.F.10
Torroni, A.11
-
31
-
-
0034778633
-
Detecting errors in mtDNA data by phylogenetic analysis
-
PMID: 11724431
-
Bandelt HJ, Lahermo P, Richards M, Macaulay V. Detecting errors in mtDNA data by phylogenetic analysis. Int J Legal Med 2001; 115:64-69. [PMID: 11724431]
-
(2001)
Int J Legal Med
, vol.115
, pp. 64-69
-
-
Bandelt, H.J.1
Lahermo, P.2
Richards, M.3
Macaulay, V.4
-
32
-
-
1842614835
-
A call for mtDNA data quality control in forensic science
-
PMID: 15066707
-
Yao YG, Bravi CM, Bandelt HJ. A call for mtDNA data quality control in forensic science. Forensic Sci Int 2004; 141:1-6. [PMID: 15066707]
-
(2004)
Forensic Sci Int
, vol.141
, pp. 1-6
-
-
Yao, Y.G.1
Bravi, C.M.2
Bandelt, H.J.3
-
33
-
-
0034529047
-
Evolutionary history of the mtDNA 9-bp deletion in Chinese populations and its relevance to the peopling of east and southeast Asia
-
PMID: 11140950
-
Yao YG, Watkins WS, Zhang YP. Evolutionary history of the mtDNA 9-bp deletion in Chinese populations and its relevance to the peopling of east and southeast Asia. Hum Genet 2000; 107:504-512. [PMID: 11140950]
-
(2000)
Hum Genet
, vol.107
, pp. 504-512
-
-
Yao, Y.G.1
Watkins, W.S.2
Zhang, Y.P.3
-
34
-
-
0031015048
-
Down-regulation of mammalian mitochondrial RNAs during oxidative stress
-
PMID: 8981048
-
Crawford DR, Wang Y, School GP, Kochheiser J, Davies KGPJ. Down-regulation of mammalian mitochondrial RNAs during oxidative stress. Free Radic Biol Med 1997; 22:551-559. [PMID: 8981048]
-
(1997)
Free Radic Biol Med
, vol.22
, pp. 551-559
-
-
Crawford, D.R.1
Wang, Y.2
School, G.P.3
Kochheiser, J.4
Davies, K.G.P.J.5
-
35
-
-
0034025592
-
F(2) isoprostanes, potential specific markers of oxidative damage in human retina
-
PMID: 10828732
-
Nourooz-Zadeh J, Pereira P. F(2) isoprostanes, potential specific markers of oxidative damage in human retina. Ophthalmic Res 2000; 32:133-137. [PMID: 10828732]
-
(2000)
Ophthalmic Res
, vol.32
, pp. 133-137
-
-
Nourooz-Zadeh, J.1
Pereira, P.2
-
36
-
-
0021331799
-
Basic mechanisms underlying the production of photochemical lesions in the mammalian retina
-
PMID: 6690219
-
Ham WT Jr, Mueller HA, Ruffolo JJ Jr, Millen JE, Cleary SF, Guerry RK, Guerry D 3rd. Basic mechanisms underlying the production of photochemical lesions in the mammalian retina. Curr Eye Res 1984; 3:165-174. [PMID: 6690219]
-
(1984)
Curr Eye Res
, vol.3
, pp. 165-174
-
-
Ham Jr., W.T.1
Mueller, H.A.2
Ruffolo Jr., J.J.3
Millen, J.E.4
Cleary, S.F.5
Guerry, R.K.6
Guerry, D.7
-
37
-
-
0031762824
-
Lipid peroxidation products and antioxidants in human disease
-
PMID: 9788902
-
Romero FJ, Bosch-Morell F, Romero MJ, Jareno EJ, Romero B, Marin N, Roma J. Lipid peroxidation products and antioxidants in human disease. Environ Health Perspect 1998; 106:1229-1234. [PMID: 9788902]
-
(1998)
Environ Health Perspect
, vol.106
, pp. 1229-1234
-
-
Romero, F.J.1
Bosch-Morell, F.2
Romero, M.J.3
Jareno, E.J.4
Romero, B.5
Marin, N.6
Roma, J.7
-
38
-
-
68949089961
-
OPA1 functions in mitochondria and dysfunctions in optic nerve
-
PMID: 19389483
-
Lenaers G, Reynier P, Elachouri G, Soukkarieh C, Olichon A, Belenguer P, Baricault L, Ducommun B, Hamel C, Delettre C. OPA1 functions in mitochondria and dysfunctions in optic nerve. Int J Biochem Cell Biol 2009; 41:1866-1874. [PMID: 19389483]
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(2009)
Int J Biochem Cell Biol
, vol.41
, pp. 1866-1874
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Lenaers, G.1
Reynier, P.2
Elachouri, G.3
Soukkarieh, C.4
Olichon, A.5
Belenguer, P.6
Baricault, L.7
Ducommun, B.8
Hamel, C.9
Delettre, C.10
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