Recurrent mutations in theCDKL5gene: Genotype-phenotype relationships-Reference-Cited by-同舟云学术

Recurrent mutations in theCDKL5gene: Genotype-phenotype relationships

Published:2012-06-07 Issue:7 Volume:158A Page:1612-1619
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Bahi-Buisson Nadia,Villeneuve Nathalie,Caietta Emilie,Jacquette Aurélia,Maurey Helene,Matthijs Gert,Van Esch Hilde,Delahaye Andrée,Moncla Anne,Milh Mathieu,Zufferey Flore,Diebold Bertrand,Bienvenu Thierry

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference35 articles.

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3. Early onset seizure variant of Rett syndrome: Definition of the clinical diagnostic criteria;Artuso;Brain Dev,2010

4. The three stages of epilepsy in patients with CDKL5 mutations;Bahi-Buisson;Epilepsia,2008a

5. Key clinical features to identify girls with CDKL5 mutations;Bahi-Buisson;Brain,2008b

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