NYX mutations in four families with high myopia with or without CSNB1
about
Caucasian Families Exhibit Significant Linkage of Myopia to Chromosome 11p.Novel TRPM1 mutations in two Chinese families with early-onset high myopia, with or without complete congenital stationary night blindness.The Transduction Cascade in Retinal ON-Bipolar Cells: Signal Processing and Disease.Myopia in Chinese families shows linkage to 10q26.13.
P2860
NYX mutations in four families with high myopia with or without CSNB1
description
2015 nî lūn-bûn
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2015 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի մարտին հրատարակված գիտական հոդված
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2015年の論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年论文
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name
NYX mutations in four families with high myopia with or without CSNB1
@ast
NYX mutations in four families with high myopia with or without CSNB1
@en
type
label
NYX mutations in four families with high myopia with or without CSNB1
@ast
NYX mutations in four families with high myopia with or without CSNB1
@en
prefLabel
NYX mutations in four families with high myopia with or without CSNB1
@ast
NYX mutations in four families with high myopia with or without CSNB1
@en
P2093
P2860
P1433
P1476
NYX mutations in four families with high myopia with or without CSNB1
@en
P2093
P2860
P304
P577
2015-03-05T00:00:00Z