De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: a genomics approach to personalized medicine.
about
Monoamine oxidase A and A/B knockout mice display autistic-like features.XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition.Mutations in monoamine oxidase (MAO) genes in mice lead to hypersensitivity to serotonin-enhancing drugs: implications for drug side effects in humansMonoamine neurotransmitter disorders--clinical advances and future perspectives.
P2860
De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: a genomics approach to personalized medicine.
description
2012 nî lūn-bûn
@nan
2012 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2012年の論文
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2012年学术文章
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2012年学术文章
@zh-cn
2012年学术文章
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2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
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name
De novo microdeletion of Xp11. ...... oach to personalized medicine.
@ast
De novo microdeletion of Xp11. ...... oach to personalized medicine.
@en
type
label
De novo microdeletion of Xp11. ...... oach to personalized medicine.
@ast
De novo microdeletion of Xp11. ...... oach to personalized medicine.
@en
prefLabel
De novo microdeletion of Xp11. ...... oach to personalized medicine.
@ast
De novo microdeletion of Xp11. ...... oach to personalized medicine.
@en
P2093
P2860
P1476
De novo microdeletion of Xp11. ...... oach to personalized medicine.
@en
P2093
Jean C Shih
John M Graham
Keith Hyland
Nancy Kramer
Ryan E O'Leary
Y Jane Tavyev Asher
P2860
P304
P356
10.1016/J.EJMG.2012.01.007
P577
2012-02-03T00:00:00Z