Loss of function of KIAA2022 causes mild to severe intellectual disability with an autism spectrum disorder and impairs neurite outgrowth-Reference-Cited by-同舟云学术

Loss of function of KIAA2022 causes mild to severe intellectual disability with an autism spectrum disorder and impairs neurite outgrowth

Published:2013-04-24 Issue:16 Volume:22 Page:3306-3314
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Van Maldergem Lionel,Hou Qingming,Kalscheuer Vera M.,Rio Marlène,Doco-Fenzy Martine,Medeira Ana,de Brouwer Arjan P.M.,Cabrol Christelle,Haas Stefan A.,Cacciagli Pierre,Moutton Sébastien,Landais Emilie,Motte Jacques,Colleaux Laurence,Bonnet Céline,Villard Laurent,Dupont Juliette,Man Heng-Ye

Publisher

Oxford University Press (OUP)

Subject

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

Link

http://academic.oup.com/hmg/article-pdf/22/16/3306/17260083/ddt187.pdf

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3. Genomic microarrays in mental retardation: a practical workflow for diagnostic applications;Koolen;Hum. Mutat.,2009

4. Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing;Hu;Hugo J.,2009

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