PRUNE is crucial for normal brain development and mutated in microcephaly with neurodevelopmental impairment
about
Potential Role of Microtubule Stabilizing Agents in Neurodevelopmental Disorders.Reply: PRUNE1: a disease-causing gene for secondary microcephaly.PRUNE1: a disease-causing gene for secondary microcephaly.A homozygous loss-of-function mutation in PDE2A associated to early-onset hereditary chorea.Reply: The phenotypic and molecular spectrum of PEHO syndrome and PEHO-like disorders.The phenotypic and molecular spectrum of PEHO syndrome and PEHO-like disorders.PRUNE Syndrome Is a New Neurodevelopmental Disorder: Report and Review.The Role of the Microtubule Cytoskeleton in Neurodevelopmental Disorders.
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P2860
PRUNE is crucial for normal brain development and mutated in microcephaly with neurodevelopmental impairment
description
2017 nî lūn-bûn
@nan
2017 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2017 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2017年の論文
@ja
2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
@wuu
name
PRUNE is crucial for normal br ...... neurodevelopmental impairment
@ast
PRUNE is crucial for normal br ...... neurodevelopmental impairment
@en
type
label
PRUNE is crucial for normal br ...... neurodevelopmental impairment
@ast
PRUNE is crucial for normal br ...... neurodevelopmental impairment
@en
prefLabel
PRUNE is crucial for normal br ...... neurodevelopmental impairment
@ast
PRUNE is crucial for normal br ...... neurodevelopmental impairment
@en
P2093
P2860
P50
P921
P356
P1433
P1476
PRUNE is crucial for normal br ...... neurodevelopmental impairment
@en
P2093
Ahmed Al-Amri
Aisha Al-Khayat
Andrew H Crosby
Angela Di Somma
Angela Duilio
Anna Rajab
Atieh Eslahi
Carmela Scuderi
Ender Karaca
Eugenia Borgione
P2860
P304
P356
10.1093/BRAIN/AWX014
P407
P577
2017-04-01T00:00:00Z