Symptomatic abnormalities of dark adaptation in patients with EFEMP1 retinal dystrophy (Malattia Leventinese/Doyne honeycomb retinal dystrophy).
about
ABCA4-associated retinal degenerations spare structure and function of the human parapapillary retina.A novel haplotype with the R345W mutation in the EFEMP1 gene associated with autosomal dominant drusen in a Japanese family.A CTRP5 gene S163R mutation knock-in mouse model for late-onset retinal degeneration
P2860
Symptomatic abnormalities of dark adaptation in patients with EFEMP1 retinal dystrophy (Malattia Leventinese/Doyne honeycomb retinal dystrophy).
description
2002 nî lūn-bûn
@nan
2002 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Symptomatic abnormalities of d ...... honeycomb retinal dystrophy).
@ast
Symptomatic abnormalities of d ...... honeycomb retinal dystrophy).
@en
type
label
Symptomatic abnormalities of d ...... honeycomb retinal dystrophy).
@ast
Symptomatic abnormalities of d ...... honeycomb retinal dystrophy).
@en
prefLabel
Symptomatic abnormalities of d ...... honeycomb retinal dystrophy).
@ast
Symptomatic abnormalities of d ...... honeycomb retinal dystrophy).
@en
P2093
P2860
P356
P1433
P1476
Symptomatic abnormalities of d ...... e honeycomb retinal dystrophy)
@en
P2093
P2860
P2888
P356
10.1038/SJ.EYE.6700018
P577
2002-01-01T00:00:00Z
P5875
P6179
1048078662