Mutation spectra in autosomal dominant and recessive retinitis pigmentosa in northern Sweden.
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Characterization of macular structure and function in two Swedish families with genetically identified autosomal dominant retinitis pigmentosaA novel PRPF31 mutation in a large Chinese family with autosomal dominant retinitis pigmentosa and macular degeneration.Mammalian diseases of phosphatidylinositol transfer proteins and their homologs.
P2860
Mutation spectra in autosomal dominant and recessive retinitis pigmentosa in northern Sweden.
description
2010 nî lūn-bûn
@nan
2010 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Mutation spectra in autosomal ...... pigmentosa in northern Sweden.
@ast
Mutation spectra in autosomal ...... pigmentosa in northern Sweden.
@en
type
label
Mutation spectra in autosomal ...... pigmentosa in northern Sweden.
@ast
Mutation spectra in autosomal ...... pigmentosa in northern Sweden.
@en
prefLabel
Mutation spectra in autosomal ...... pigmentosa in northern Sweden.
@ast
Mutation spectra in autosomal ...... pigmentosa in northern Sweden.
@en
P2093
P2860
P1476
Mutation spectra in autosomal ...... pigmentosa in northern Sweden.
@en
P2093
Linda Köhn
Marie Burstedt
Ola Sandgren
P2860
P304
P356
10.1007/978-1-4419-1399-9_29
P407
P577
2010-01-01T00:00:00Z