FOXG1 Is Responsible for the Congenital Variant of Rett Syndrome-Reference-Cited by-同舟云学术

FOXG1 Is Responsible for the Congenital Variant of Rett Syndrome

Published:2008-07 Issue:1 Volume:83 Page:89-93
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Ariani Francesca,Hayek Giuseppe,Rondinella Dalila,Artuso Rosangela,Mencarelli Maria Antonietta,Spanhol-Rosseto Ariele,Pollazzon Marzia,Buoni Sabrina,Spiga Ottavia,Ricciardi Sara,Meloni Ilaria,Longo Ilaria,Mari Francesca,Broccoli Vania,Zappella Michele,Renieri Alessandra

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference27 articles.

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3. Preserved speech variant is allelic of classic Rett syndrome;De Bona;Eur. J. Hum. Genet.,2000

4. Mutations in the X-linked cyclin-dependent kinase-like 5 (CDKL5/STK9) gene are associated with severe neurodevelopmental retardation;Tao;Am. J. Hum. Genet.,2004

5. CDKL5/STK9 is mutated in Rett syndrome variant with infantile spasms;Scala;J. Med. Genet.,2005

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