Two novel mutations in the EIF2AK3 gene in children with Wolcott-Rallison syndrome.
about
Translational control by eIF2α kinases in long-lasting synaptic plasticity and long-term memory.Brain-specific disruption of the eIF2α kinase PERK decreases ATF4 expression and impairs behavioral flexibility.Frequency and spectrum of Wolcott-Rallison syndrome in Saudi Arabia: a systematic review.The eIF2α kinase PERK limits the expression of hippocampal metabotropic glutamate receptor-dependent long-term depression.Permanent neonatal diabetes mellitus - a case report of a rare cause of diabetes mellitus in East AfricaA Novel Single-Nucleotide Deletion (c.1020delA) in NSUN2 Causes Intellectual Disability in an Emirati Child.Recurrent Hepatitis in Two Iranian Children: A Novel (Q166R) Mutation in EIF2AK3 Leading to Wolcott-Rallison Syndrome.
P2860
Q30429927-3A94E6B3-5BCF-4B4B-959E-9F29FB4EA0FFQ30465575-C3D530B2-763F-4764-A3A8-4D21864358A2Q34350361-58DC6256-4D18-4277-BC11-6B595A58C22CQ37714851-22383A5B-9E1C-4EE0-828F-4B90B13D2B34Q38612681-7B2E9833-59E7-45B2-BD05-7F79EAEA2FE8Q40857594-5FB23013-A2B9-4D3A-B96B-D39563FD3B2BQ42580490-73053BB2-3A50-44AA-98DA-3AE9338B4ED0
P2860
Two novel mutations in the EIF2AK3 gene in children with Wolcott-Rallison syndrome.
description
2010 nî lūn-bûn
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2010年の論文
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2010年学术文章
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2010年学术文章
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2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
2010年學術文章
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2010年學術文章
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name
Two novel mutations in the EIF2AK3 gene in children with Wolcott-Rallison syndrome.
@en
Two novel mutations in the EIF2AK3 gene in children with Wolcott-Rallison syndrome.
@nl
type
label
Two novel mutations in the EIF2AK3 gene in children with Wolcott-Rallison syndrome.
@en
Two novel mutations in the EIF2AK3 gene in children with Wolcott-Rallison syndrome.
@nl
prefLabel
Two novel mutations in the EIF2AK3 gene in children with Wolcott-Rallison syndrome.
@en
Two novel mutations in the EIF2AK3 gene in children with Wolcott-Rallison syndrome.
@nl
P2093
P2860
P1433
P1476
Two novel mutations in the EIF2AK3 gene in children with Wolcott-Rallison syndrome.
@en
P2093
André F Reis
Bernard Grandchamp
Carolina Oliveira
Caroline Kannengiesser
Claire Oudin
Farida Jennane
Fernando Kok
Gilberto Velho
Nadir Cheurfa
Roberta Diaz Savoldelli
P2860
P304
P356
10.1111/J.1399-5448.2010.00679.X
P433
P577
2010-09-07T00:00:00Z