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Article

DYRK1B variant linked to autosomal dominant metabolic syndrome.

Clinical genetics - 1 Jan 2015

Hickmott J

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Share to Genetic Predisposition to Disease
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Identifiers

PMID: 25092113
DOI: 10.1111/cge.12477

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DYRK1B variant linked to autosomal dominant metabolic syndrome.PMID 25092113Read ↗

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Genetics: Founder mutations identified in an inherited form of the metabolic syndrome.Semantic proximity Read ↗

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Function and regulation of Dyrk1A: towards understanding Down syndromeSemantic proximity Read ↗

DYRK1A: a down syndrome-related dual protein kinase with a versatile role in tumorigenesisSemantic proximity Read ↗

Intragenic deletion in DYRK1A leads to mental retardation and primary microcephaly.Semantic proximity Read ↗

DYRK1B mutations associated with metabolic syndrome impair the chaperone-dependent maturation of the kinase domain.Semantic proximity Read ↗

DYRK1A-related intellectual disability: a syndrome associated with congenital anomalies of the kidney and urinary tractSemantic proximity Read ↗

The Omnipresence of DYRK1A in Human DiseasesSemantic proximity Read ↗

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