메뉴 건너뛰기




Volumn 5, Issue 1, 1996, Pages 17-26

Controversies in counseling for mitochondrial conditions

Author keywords

Genetic counseling; Mitochondrial disorders; Retinitis pigmentosa

Indexed keywords


EID: 0344355792     PISSN: 10597700     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF01408662     Document Type: Article
Times cited : (1)

References (23)
  • 2
    • 0024146932 scopus 로고
    • Biogenesis of mitochondria
    • Attardi G, Schatz G (1988) Biogenesis of mitochondria. Annu Rev Cell Biol 4:289-333.
    • (1988) Annu Rev Cell Biol , vol.4 , pp. 289-333
    • Schatz G, A.G.1
  • 3
    • 0027497228 scopus 로고
    • Identical mitochondrial DNA deletion in mother with progressive external ophthalmoplegia and son with Pearson marrow-pancreas syndrome
    • Bernes SM, Bacino CB, Prezant TR, Pearson MA, Wood TS, Fournier P, Fischel-Ghodsian N (1992) Identical mitochondrial DNA deletion in mother with progressive external ophthalmoplegia and son with Pearson marrow-pancreas syndrome. / Pediat 123:598-602,
    • (1992) / Pediat , vol.123 , pp. 598-602
    • Bernes, S.M.1    Bacino, C.B.2    Prezant, T.R.3    Pearson, M.A.4    Wood, T.S.5    Fournier, P.6    Fischel-Ghodsian, N.7
  • 6
    • 0026555299 scopus 로고
    • Mitochondrial disorders in pediatrics
    • Clarke LA (1992) Mitochondrial disorders in pediatrics. Pediat Clin N Am 39(2):319-334.
    • (1992) Pediat Clin N Am , vol.39 , Issue.2 , pp. 319-334
    • Clarke, L.A.1
  • 11
    • 0017838513 scopus 로고
    • Retinitis pigmentosa: Genetic percentages
    • Fishman GA (1978) Retinitis pigmentosa: Genetic percentages. Arch Ophthalmol 96:822-826.
    • (1978) Arch Ophthalmol , vol.96 , pp. 822-826
    • Fishman, G.A.1
  • 14
    • 0021909244 scopus 로고
    • Nucleotide sequence preservation of human mitochondrial DNA
    • Monnat RJ, Loeb LA (1985) Nucleotide sequence preservation of human mitochondrial DNA. Proc Natl Acad Sci USA 82:2895-2899.
    • (1985) Proc Natl Acad Sci USA , vol.82 , pp. 2895-2899
    • Monnat, R.J.1    Loeb, L.A.2
  • 16
    • 0025881563 scopus 로고
    • The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation
    • Newman NJ, Lott MT, Wallace DC (1991) The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation. Am J Ophthalmol 111:750-762.
    • (1991) Am J Ophthalmol , vol.111 , pp. 750-762
    • Newman, N.J.1    Lott, M.T.2    Wallace, D.C.3
  • 17
    • 26044460651 scopus 로고
    • Deficiency in NADP dehydrogenase and cytochrome b in a patient with a familial mitochondrial myopathy
    • abstract 2208
    • Nigro MA, Johns DR, Lee CP, Taang S, Rauchova H, Chang CH, Paridon S (1991) Deficiency in NADP dehydrogenase and cytochrome b in a patient with a familial mitochondrial myopathy. Neurology 41 (suppl. 1 abstract 2208)178.
    • (1991) Neurology , vol.41 , Issue.1 SUPPL. , pp. 178
    • Nigro, M.A.1    Johns, D.R.2    Lee, C.P.3    Taang, S.4    Rauchova, H.5    Ch, C.6    Paridon, S.7
  • 18
    • 0026759746 scopus 로고
    • Mitochondrial diseases
    • Nonaka I (1992) Mitochondrial diseases (review). Curr Opin Neurol Neurosurg 5(5):622-632.
    • (1992) Curr Opin Neurol Neurosurg , vol.5 , Issue.5 , pp. 622-632
    • Nonaka, I.1
  • 19
  • 20
    • 0027441181 scopus 로고
    • Variable retinal and neurological manifestations in patients harboring the mitochondrial DNA 8993 mutation
    • Ortiz RG, Newman NJ, Shoffner JM, Kaufman AE, Koontz DA, Wallace DC (1993) Variable retinal and neurological manifestations in patients harboring the mitochondrial DNA 8993 mutation. Arch Ophthalmol 111(11):1525-1530.
    • (1993) Arch Ophthalmol , vol.111 , Issue.11 , pp. 1525-1530
    • Ortiz, R.G.1    Newman, N.J.2    Shoffner, J.M.3    Kaufman, A.E.4    Koontz, D.A.5    Wallace, D.C.6
  • 23
    • 26044481508 scopus 로고
    • personal communication
    • Shoffner J (1994) (personal communication).
    • (1994)
    • Shoffner, J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.