WS1 gene mutation analysis of Wolfram syndrome in a Chinese patient and a systematic review of literatures.
about
Impairment of visual function and retinal ER stress activation in Wfs1-deficient mice.Phenotype Prediction of Pathogenic Nonsynonymous Single Nucleotide Polymorphisms in WFS1A Challenging Form of Non-autoimmune Insulin-Dependent Diabetes in a Wolfram Syndrome Patient with a Novel Sequence Variant.Clinical Characteristics of Wolfram Syndrome in Chinese Population and a Novel Frameshift Mutation in WFS1.
P2860
WS1 gene mutation analysis of Wolfram syndrome in a Chinese patient and a systematic review of literatures.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 23 October 2010
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
WS1 gene mutation analysis of ...... tematic review of literatures.
@en
WS1 gene mutation analysis of ...... tematic review of literatures.
@nl
type
label
WS1 gene mutation analysis of ...... tematic review of literatures.
@en
WS1 gene mutation analysis of ...... tematic review of literatures.
@nl
prefLabel
WS1 gene mutation analysis of ...... tematic review of literatures.
@en
WS1 gene mutation analysis of ...... tematic review of literatures.
@nl
P2093
P2860
P1433
P1476
WS1 gene mutation analysis of ...... stematic review of literatures
@en
P2093
Cong-rong Gao
Zhong-jin Chen
P2860
P2888
P304
P356
10.1007/S12020-010-9350-4
P577
2010-10-23T00:00:00Z