Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex-Reference-Cited by-同舟云学术

Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex

Published:2010-09-21 Issue:24 Volume:19 Page:4848-4860
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Roll Patrice,Vernes Sonja C.,Bruneau Nadine,Cillario Jennifer,Ponsole-Lenfant Magali,Massacrier Annick,Rudolf Gabrielle,Khalife Manal,Hirsch Edouard,Fisher Simon E.,Szepetowski Pierre

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/19/24/4848/13928448/ddq415.pdf

Reference43 articles.

1. On genes, speech, and language;Fisher;N. Engl. J. Med.,2009

2. FOXP2 as a molecular window into speech and language;Fisher;Trends Genet.,2009

3. A forkhead-domain gene is mutated in a severe speech and language disorder;Lai;Nature,2001

4. Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits;MacDermot;Am. J. Hum. Genet.,2005

5. Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2;Zeesman;Am. J. Med. Genet.,2006

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