Truncation of the Down Syndrome Candidate Gene DYRK1A in Two Unrelated Patients with Microcephaly-Reference-Cited by-同舟云学术

Truncation of the Down Syndrome Candidate Gene DYRK1A in Two Unrelated Patients with Microcephaly

Published:2008-05 Issue:5 Volume:82 Page:1165-1170
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Møller Rikke S.,Kübart Sabine,Hoeltzenbein Maria,Heye Babett,Vogel Ida,Hansen Christian P.,Menzel Corinna,Ullmann Reinhard,Tommerup Niels,Ropers Hans-Hilger,Tümer Zeynep,Kalscheuer Vera M.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference24 articles.

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3. Dyrk1A haploinsufficiency affects viability and causes developmental delay and abnormal brain morphology in mice;Fotaki;Mol. Cell. Biol.,2002

4. Haploinsufficiency of Dyrk1A in mice leads to specific alterations in the development and regulation of motor activity;Fotaki;Behav. Neurosci.,2004

5. Dopaminergic deficiency in mice with reduced levels of the dual-specificity tyrosine-phosphorylated and regulated kinase 1A, Dyrk1A(+/−);Martinez de Lagran;Genes Brain Behav.,2007

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