Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits-Reference-Cited by-同舟云学术

Identification of FOXP2 Truncation as a Novel Cause of Developmental Speech and Language Deficits

Published:2005-06 Issue:6 Volume:76 Page:1074-1080
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

MacDermot Kay D.,Bonora Elena,Sykes Nuala,Coupe Anne-Marie,Lai Cecilia S.L.,Vernes Sonja C.,Vargha-Khadem Faraneh,McKenzie Fiona,Smith Robert L.,Monaco Anthony P.,Fisher Simon E.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

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5. Molecular evolution of FOXP2, a gene involved in speech and language;Enard;Nature,2002

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