Establishing risk of vision loss in Leber hereditary optic neuropathy-Reference-Cited by-同舟云学术

Establishing risk of vision loss in Leber hereditary optic neuropathy

Published:2021-11 Issue:11 Volume:108 Page:2159-2170
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Lopez Sanchez M. Isabel G.,Kearns Lisa S.,Staffieri Sandra E.,Clarke Linda,McGuinness Myra B.,Meteoukki Wafaa,Samuel Sona,Ruddle Jonathan B.,Chen Celia,Fraser Clare L.,Harrison John,Hewitt Alex W.,Howell Neil,Mackey David A.^ORCID

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference50 articles.

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2. Mitochondrial DNA mutation associated with Leber’s hereditary optic neuropathy;Wallace;Science,1988

3. An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy;Johns;Biochem. Biophys. Res. Commun.,1992

4. A variant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology;Mackey;Am. J. Hum. Genet.,1992

5. Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees;Howell;Am. J. Hum. Genet.,1991

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