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PMID: 21294719 Published · ppublish English Case Reports Letter Research Support, Non-U.S. Gov't

Intragenic deletion in DYRK1A leads to mental retardation and primary microcephaly.

Clinical genetics ·Vol. 79 ·No. 3 ·2011-03-00 ·Pages 296-9

van Bon BW, Hoischen A, Hehir-Kwa J, de Brouwer AP, Ruivenkamp C, Gijsbers AC, Marcelis CL, de Leeuw N, Veltman JA, Brunner HG, de Vries BB

Abstract

暂无摘要

MeSH Terms

Adult Child Female Gene Deletion Genetic Association Studies Heterozygote Humans Infant Intellectual Disability/genetics Male Microcephaly/genetics Phenotype Protein Serine-Threonine Kinases/genetics Protein-Tyrosine Kinases/genetics

Chemicals

Dyrk kinase Protein-Tyrosine Kinases Protein Serine-Threonine Kinases

Authors & Affiliations

11 authors, click to expand affiliations / ORCID

van Bon B W M

Hoischen A

Hehir-Kwa J

de Brouwer A P M

Ruivenkamp C

Gijsbers A C J

Marcelis C L

de Leeuw N

Veltman J A

Brunner H G

de Vries B B A

Article Info

Journal

Clinical genetics

Abbr.

Clin Genet

ISSN

1399-0004

DOI

10.1111/j.1399-0004.2010.01544.x

Published

2011-03-00

Pages

296-9

Language

English

Region

Denmark

NLM ID

0253664

Subset

External Links

PubMed source DOI: 10.1111/j.1399-0004.2010.01544.x View journal details

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Intragenic deletion in DYRK1A leads to mental retardation and primary microcephaly.

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