Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 function-Reference-Cited by-同舟云学术

Mutations in human C2CD3 cause skeletal dysplasia and provide new insights into phenotypic and cellular consequences of altered C2CD3 function

Published:2016-04-20 Issue:1 Volume:6 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Cortés Claudio R.,McInerney-Leo Aideen M.,Vogel Ida,Rondón Galeano Maria C.,Leo Paul J.,Harris Jessica E.,Anderson Lisa K.,Keith Patricia A.,Brown Matthew A.,Ramsing Mette,Duncan Emma L.,Zankl Andreas,Wicking Carol

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep24083.pdf

Reference42 articles.

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