Identification of Nine New RAI1-Truncating Mutations in Smith-Magenis Syndrome Patients without 17p11.2 Deletions.
about
Rai1 frees mice from the repression of active wake behaviors by light.Whole exome sequencing identifies RAI1 mutation in a morbidly obese child diagnosed with ROHHAD syndromeFine mapping of bone structure and strength QTLs in heterogeneous stock rat.Molecular and Neural Functions of Rai1, the Causal Gene for Smith-Magenis Syndrome.RAI1 gene mutations: mechanisms of Smith-Magenis syndrome.A Rare De Novo RAI1 Gene Mutation Affecting BDNF-Enhancer-Driven Transcription Activity Associated with Autism and Atypical Smith-Magenis Syndrome Presentation.
P2860
Identification of Nine New RAI1-Truncating Mutations in Smith-Magenis Syndrome Patients without 17p11.2 Deletions.
description
2014 nî lūn-bûn
@nan
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
2014年论文
@zh
2014年论文
@zh-cn
name
Identification of Nine New RAI ...... nts without 17p11.2 Deletions.
@en
type
label
Identification of Nine New RAI ...... nts without 17p11.2 Deletions.
@en
prefLabel
Identification of Nine New RAI ...... nts without 17p11.2 Deletions.
@en
P2093
P2860
P356
P1476
Identification of Nine New RAI ...... nts without 17p11.2 Deletions.
@en
P2093
A Jacquette
C Barthélémy
C Bendavid
F Bonnet-Brilhault
P2860
P356
10.1159/000357359
P577
2014-01-07T00:00:00Z