Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5-Reference-Cited by-同舟云学术

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with a loss-of-function mutation in CDK5

Published:2015-01-06 Issue:3 Volume:134 Page:305-314
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Magen Daniella,Ofir Ayala,Berger Liron,Goldsher Dorit,Eran Ayelet,Katib Nassser,Nijem Yousif,Vlodavsky Euvgeni,Zur Shay,Behar Doron M.,Fellig Yakov,Mandel Hanna

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-014-1522-5.pdf

Reference39 articles.

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5. Bond J, Roberts E, Springell K, Lizarraga S, Scott S, Higgins J, Hampshire DJ, Morrison EE, Leal GF, Silva EO et al (2005) A centrosomal mechanism involving CDK5RAP2 and CENPJ controls brain size. Nat Genet 37:353–355. doi: 10.1038/ng1539

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