Genetic localisation of the RP2 type of X linked retinitis pigmentosa in a large kindred.

Genetic linkage and deletion studies have led to the proposal that there are at least two loci on the X chromosome which are responsible for X linked retinitis pigmentosa (XLRP). One locus (RP3) has been closely defined by genetic linkage and deletion analyses and localised to the region between the...

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Detaylı Bibliyografya
Asıl Yazarlar: Wright, A F, Bhattacharya, S S, Aldred, M A, Jay, M, Carothers, A D, Thomas, N S, Bird, A C, Jay, B, Evans, H J
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1991
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1016954/
https://ncbi.nlm.nih.gov/pubmed/1895315
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