TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis.
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Novel compound heterozygous variants in PLK4 identified in a patient with autosomal recessive microcephaly and chorioretinopathy.The α-Tubulin gene TUBA1A in Brain Development: A Key Ingredient in the Neuronal Isotype Blend.Clinical and Functional Characterization of the Recurrent TUBA1A p.(Arg2His) Mutation
P2860
TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis.
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2015 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
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2015 թվականի հոտեմբերին հրատարակված գիտական հոդված
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2015年の論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年論文
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2015年论文
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TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis.
@ast
TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis.
@en
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label
TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis.
@ast
TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis.
@en
prefLabel
TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis.
@ast
TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis.
@en
P2093
P2860
P356
P1433
P1476
TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis.
@en
P2093
Fuyuki Miya
Hiroki Kurahashi
Hiroyuki Yamamoto
Itaru Yanagihara
Jun Natsume
Kenjiro Kosaki
Makiko Tsutsumi
Mami Yamasaki
Naoko Fujita
Naoko Ishihara
P2860
P2888
P356
10.1038/SREP15165
P407
P577
2015-10-23T00:00:00Z
P5875
P6179
1030585005