A gene for X-linked optic atrophy is closely linked to the Xp11.4-Xp11.2 region of the X chromosome.

The aim of this study was to identify the chromosomal location of the disease-causing gene in a family apparently segregating X-linked optic atrophy. A large family of 45 individuals with a four-generation history of X-linked optic atrophy was reexamined in a full ophthalmic as well as electrophysio...

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Main Authors: Assink, J J, Tijmes, N T, ten Brink, J B, Oostra, R J, Riemslag, F C, de Jong, P T, Bergen, A A
Format: Artigo
Jezik:Inglês
Izdano: 1997
Teme:
Research Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1715990/
https://ncbi.nlm.nih.gov/pubmed/9382106
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