Biallelic mutations in human DCC cause developmental split-brain syndrome.

Biallelic mutations in human DCC cause developmental split-brain syndrome.

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http://www.wikidata.org/entity/Q38934779
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

Biallelic mutations in human DCC cause developmental split-brain syndrome.

Item
http://www.wikidata.org/entity/Q38934779
description
2017 nî lūn-bûn
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2017年の論文
@ja
2017年学术文章
@wuu
2017年学术文章
@zh-cn
2017年学术文章
@zh-hans
2017年学术文章
@zh-my
2017年学术文章
@zh-sg
2017年學術文章
@yue
2017年學術文章
@zh
2017年學術文章
@zh-hant
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
P1433
P1476
P2093
P2860
P2888
P304
P31
P356
P407
P433
P478
P50
P577
P698
P932
P356
P1433
P1476
Biallelic mutations in human DCC cause developmental split-brain syndrome
@en
P2093
P2860
P2888
P304
P31
P356
P407
P433
P478
P50
P577
P698
P932