Biallelic mutations in human DCC cause developmental split-brain syndrome.
about
DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development.Genome-wide analysis in UK Biobank identifies four loci associated with mood instability and genetic correlation with major depressive disorder, anxiety disorder and schizophrenia.Making Dopamine Connections in Adolescence.DCC mutation update: Congenital mirror movements, isolated agenesis of the corpus callosum, and developmental split brain syndrome.Mutations in the netrin-1 gene cause congenital mirror movements.Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencing.Brain Tumor promotes axon growth across the midline through interactions with the microtubule stabilizing protein Apc2.Next-generation sequencing analysis of multiplex families with atypical psychosis
P2860
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P2860
Biallelic mutations in human DCC cause developmental split-brain syndrome.
description
2017 nî lūn-bûn
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2017年の論文
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年學術文章
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2017年學術文章
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2017年學術文章
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name
Biallelic mutations in human DCC cause developmental split-brain syndrome.
@en
type
label
Biallelic mutations in human DCC cause developmental split-brain syndrome.
@en
prefLabel
Biallelic mutations in human DCC cause developmental split-brain syndrome.
@en
P2093
P2860
P50
P356
P1433
P1476
Biallelic mutations in human DCC cause developmental split-brain syndrome
@en
P2093
A James Barkovich
Abdullah Abu Jamea
Alissa M D'Gama
Anh-Thu N Lam
Elizabeth C Engle
Ibrahim A Alorainy
Khaled Abu-Amero
Klaus Schmitz-Abe
Marie Drottar
Mauricio R Delgado
P2860
P2888
P304
P356
10.1038/NG.3804
P407
P577
2017-02-27T00:00:00Z