WWOX and severe autosomal recessive epileptic encephalopathy: first case in the prenatal period.
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Pleiotropic Functions of Tumor Suppressor WWOX in Normal and Cancer CellsHomozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohort.W44X mutation in the WWOX gene causes intractable seizures and developmental delay: a case reportWWOX dysfunction induces sequential aggregation of TRAPPC6AΔ, TIAF1, tau and amyloid β, and causes apoptosis.Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families.Novel mutations in WWOX, RARS2, and C10orf2 genes in consanguineous Arab families with intellectual disability.Modeling WWOX Loss of Function : What Have We Learned?WWOX Phosphorylation, Signaling, and Role in Neurodegeneration
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WWOX and severe autosomal recessive epileptic encephalopathy: first case in the prenatal period.
description
2015 nî lūn-bûn
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2015年の論文
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
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2015年學術文章
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2015年學術文章
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name
WWOX and severe autosomal rece ...... t case in the prenatal period.
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WWOX and severe autosomal rece ...... t case in the prenatal period.
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type
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WWOX and severe autosomal rece ...... t case in the prenatal period.
@en
WWOX and severe autosomal rece ...... t case in the prenatal period.
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WWOX and severe autosomal rece ...... t case in the prenatal period.
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WWOX and severe autosomal rece ...... t case in the prenatal period.
@nl
P2093
P2860
P356
P1476
WWOX and severe autosomal rece ...... t case in the prenatal period.
@en
P2093
Bénédicte François
Christophe Philippe
Emmanuelle Schmitt
Jean Pierre Masutti
Laetitia Lambert
Mireille Vibert
Mylène Valduga
Pascale Bach-Segura
Patrick Pinaud
Philippe Jonveaux
P2860
P2888
P304
P356
10.1038/JHG.2015.17
P577
2015-02-26T00:00:00Z