A null mutation in TNIK defines a novel locus for intellectual disability.
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Exome sequencing discloses KALRN homozygous variant as likely cause of intellectual disability and short stature in a consanguineous pedigreeThe Molecular Genetics of Autosomal Recessive Nonsyndromic Intellectual Disability: a Mutational Continuum and Future Recommendations.Rap2 and TNIK control Plexin-dependent tiled synaptic innervation in
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A null mutation in TNIK defines a novel locus for intellectual disability.
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2016 nî lūn-bûn
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2016年の論文
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2016年学术文章
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2016年学术文章
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A null mutation in TNIK defines a novel locus for intellectual disability.
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A null mutation in TNIK defines a novel locus for intellectual disability.
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label
A null mutation in TNIK defines a novel locus for intellectual disability.
@en
A null mutation in TNIK defines a novel locus for intellectual disability.
@nl
prefLabel
A null mutation in TNIK defines a novel locus for intellectual disability.
@en
A null mutation in TNIK defines a novel locus for intellectual disability.
@nl
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A null mutation in TNIK defines a novel locus for intellectual disability.
@en
P2093
Dhekra AlNaqeb
Dorota Monies
Hanan E Shamseldin
Khalid Al-Rubeaan
Mohamed Abouelhoda
Mustafa A Salih
Shams Anazi
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P2888
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P356
10.1007/S00439-016-1671-9
P577
2016-04-22T00:00:00Z