Two new Rett syndrome families and review of the literature: expanding the knowledge of MECP2 frameshift mutations.
about
Clinical review of genetic epileptic encephalopathiesFamilial cases and male cases with MECP2 mutationsMECP2 Duplication Syndrome: Evidence of Enhanced Oxidative Stress. A Comparison with Rett Syndrome.Pluripotent stem cells as a model to study non-coding RNAs function in human neurogenesis.Genetics, molecular biology, and phenotypes of x-linked epilepsy.
P2860
Two new Rett syndrome families and review of the literature: expanding the knowledge of MECP2 frameshift mutations.
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2011 nî lūn-bûn
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2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2011年の論文
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2011年学术文章
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2011年学术文章
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2011年学术文章
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2011年学术文章
@zh-my
2011年学术文章
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2011年學術文章
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name
Two new Rett syndrome families ...... of MECP2 frameshift mutations.
@ast
Two new Rett syndrome families ...... of MECP2 frameshift mutations.
@en
type
label
Two new Rett syndrome families ...... of MECP2 frameshift mutations.
@ast
Two new Rett syndrome families ...... of MECP2 frameshift mutations.
@en
prefLabel
Two new Rett syndrome families ...... of MECP2 frameshift mutations.
@ast
Two new Rett syndrome families ...... of MECP2 frameshift mutations.
@en
P2093
P2860
P921
P356
P1476
Two new Rett syndrome families ...... of MECP2 frameshift mutations
@en
P2093
Gitte Roende
Jytte B Nielsen
Kathrine Fuglsang
Kirstine Ravn
Kristin L Eiklid
Morten Duno
Ola H Skjeldal
P2860
P2888
P356
10.1186/1750-1172-6-58
P50
P5008
P577
2011-08-30T00:00:00Z
P5875
P6179
1015405174