X-linked dominant cone-rod degeneration: linkage mapping of a new locus for retinitis pigmentosa (RP 15) to Xp22.13-p22.11.

Retinitis pigmentosa is the name given to a heterogeneous group of hereditary retinal degenerations characterized by progressive visual field loss, pigmentary changes of the retina, abnormal electroretinograms, and, frequently, night blindness. In this study, we investigated a family with dominant c...

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Bibliografiske detaljer
Main Authors: McGuire, R E, Sullivan, L S, Blanton, S H, Church, M W, Heckenlively, J R, Daiger, S P
Format: Artigo
Sprog:Inglês
Udgivet: 1995
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1801245/
https://ncbi.nlm.nih.gov/pubmed/7611300
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