Exome Sequencing and Functional Analysis Identifies BANF1 Mutation as the Cause of a Hereditary Progeroid Syndrome

出版年份 2011 全文链接

标题

作者

关键词

出版物

Volume 88, Issue 5, Pages 650-656

出版商

Elsevier BV

发表日期

2011-05-09

DOI

10.1016/j.ajhg.2011.04.010

Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.

Explore

The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.

Get Started