Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture-Reference-Cited by-同舟云学术

Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture

Published:2010-10-03 Issue:11 Volume:42 Page:1015-1020
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Yu Timothy W,Mochida Ganeshwaran H,Tischfield David J,Sgaier Sema K,Flores-Sarnat Laura,Sergi Consolato M,Topçu Meral,McDonald Marie T,Barry Brenda J,Felie Jillian M,Sunu Christine,Dobyns William B,Folkerth Rebecca D,Barkovich A James,Walsh Christopher A

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.683.pdf

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5. Desmet, F.-O. et al. Human Splicing Finder: an online bioinformatics tool to predict splicing signals. Nucleic Acids Res. 37, e67 (2009).

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