Abnormal retinal thickening is a common feature among patients with ARSACS-related phenotypes
about
Novel compound heterozygous mutation in SACS gene leads to a milder autosomal recessive spastic ataxia of Charlevoix-Saguenay, ARSACS, in a Finnish family.Genetic heterogeneity of motor neuropathiesInner Retinal Dysfunction in the Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay.New practical definitions for the diagnosis of autosomal recessive spastic ataxia of Charlevoix-Saguenay.
P2860
Abnormal retinal thickening is a common feature among patients with ARSACS-related phenotypes
description
2014 nî lūn-bûn
@nan
2014 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
Abnormal retinal thickening is ...... with ARSACS-related phenotypes
@ast
Abnormal retinal thickening is ...... with ARSACS-related phenotypes
@en
Abnormal retinal thickening is ...... with ARSACS-related phenotypes
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type
label
Abnormal retinal thickening is ...... with ARSACS-related phenotypes
@ast
Abnormal retinal thickening is ...... with ARSACS-related phenotypes
@en
Abnormal retinal thickening is ...... with ARSACS-related phenotypes
@nl
prefLabel
Abnormal retinal thickening is ...... with ARSACS-related phenotypes
@ast
Abnormal retinal thickening is ...... with ARSACS-related phenotypes
@en
Abnormal retinal thickening is ...... with ARSACS-related phenotypes
@nl
P2860
P50
P1476
Abnormal retinal thickening is ...... with ARSACS-related phenotypes
@en
P2860
P356
10.1136/BJOPHTHALMOL-2013-304534
P407
P577
2014-05-01T00:00:00Z