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Phenotypic Variability Due to a Novel Glu292Lys Variation in Exon 8 of the BEST1 Gene Causing Best Macular Dystrophy

OBJECTIVE: To study the phenotypic characteristics of patients with a novel p.E292K mutation in BEST1. METHODS: Affected individuals underwent ophthalmic examination and testing that included photography, autofluorescence, OCT, and electrophysiological testing. DNA was analyzed for BEST1 mutations....

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Bibliografski detalji
Glavni autori: Sohn, Elliott H., Francis, Peter J., Duncan, Jacque L., Weleber, Richard G., Saperstein, David A., Farrell, Donald F., Stone, Edwin M.
Format: Artigo
Jezik:Inglês
Izdano: 2009
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2711525/
https://ncbi.nlm.nih.gov/pubmed/19597114
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1001/archophthalmol.2009.148
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