A novel mutation in the EIF2AK3 gene with variable expressivity in two patients with Wolcott-Rallison syndrome.
about
Evolutionary conservation and expression of human RNA-binding proteins and their role in human genetic diseaseFrequency and spectrum of Wolcott-Rallison syndrome in Saudi Arabia: a systematic review.PDIA6 regulates insulin secretion by selectively inhibiting the RIDD activity of IRE1.Liver, pancreas and kidney transplantation for the treatment of Wolcott-Rallison syndrome.Two novel mutations in the EIF2AK3 gene in children with Wolcott-Rallison syndrome.Novel mutation in wolcott-rallison syndrome with variable expression in two omani siblingsOs odontoideum in wolcott-rallison syndrome: a case series of 4 patients.Whole-Exome Sequencing Identifies One De Novo Variant in the FGD6 Gene in a Thai Family with Autism Spectrum Disorder.
P2860
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P2860
A novel mutation in the EIF2AK3 gene with variable expressivity in two patients with Wolcott-Rallison syndrome.
description
2006 nî lūn-bûn
@nan
2006 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2006 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
name
A novel mutation in the EIF2AK ...... ith Wolcott-Rallison syndrome.
@en
A novel mutation in the EIF2AK ...... ith Wolcott-Rallison syndrome.
@nl
type
label
A novel mutation in the EIF2AK ...... ith Wolcott-Rallison syndrome.
@en
A novel mutation in the EIF2AK ...... ith Wolcott-Rallison syndrome.
@nl
prefLabel
A novel mutation in the EIF2AK ...... ith Wolcott-Rallison syndrome.
@en
A novel mutation in the EIF2AK ...... ith Wolcott-Rallison syndrome.
@nl
P2093
P1433
P1476
A novel mutation in the EIF2AK ...... ith Wolcott-Rallison syndrome.
@en
P2093
F Durocher
I Bouchard
L Pelletier
R Laframboise
P356
10.1111/J.1399-0004.2006.00632.X
P577
2006-07-01T00:00:00Z