DYRK1A mutations in two unrelated patients-Reference-Cited by-同舟云学术

DYRK1A mutations in two unrelated patients

Published:2015-03 Issue:3 Volume:58 Page:168-174
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Ruaud Lyse,Mignot Cyril,Guët Agnès,Ohl Christelle,Nava Caroline,Héron Delphine,Keren Boris,Depienne Christel,Benoit Valérie,Maystadt Isabelle,Lederer Damien,Amsallem Daniel,Piard Juliette

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference22 articles.

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2. The DYRK1A gene is a cause of syndromic intellectual disability with severe microcephaly and epilepsy;Courcet;J Med Genet,2012

3. DYRK1A (dual-specificity tyrosine-phosphorylated and -regulated kinase 1A): a gene with dosage effect during development and neurogenesis;Dierssen;Sci World J,2006

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

5. Microdeletion of the Down syndrome critical region at 21q22;Fujita;Am J Med Genet Part A,2010

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