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  A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3
 
 
Title: A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3
Author: Pagnamenta, Alistair T.
Holt, Richard
Yusuf, Mohammed
Pinto, Dalila
Wing, Kirsty
Betancur, Catalina
Scherer, Stephen W.
Volpi, Emanuela V.
Monaco, Anthony P.
Appeared in: Journal of neurodevelopmental disorders
Paging: Volume 3 (2011) nr. 2 pages 124-131
Year: 2011
Contents:
Publisher: Springer US, Boston
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

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 Koninklijke Bibliotheek - National Library of the Netherlands