OPA1 disease alleles causing dominant optic atrophy have defects in cardiolipin-stimulated GTP hydrolysis and membrane tubulation

标题
OPA1 disease alleles causing dominant optic atrophy have defects in cardiolipin-stimulated GTP hydrolysis and membrane tubulation
作者
关键词
-
出版物
HUMAN MOLECULAR GENETICS
Volume 19, Issue 11, Pages 2113-2122
出版商
Oxford University Press (OUP)
发表日期
2010-02-26
DOI
10.1093/hmg/ddq088

向作者/读者发起求助以获取更多资源

Find Funding. Review Successful Grants.

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

Explore

Discover Peeref hubs

Discuss science. Find collaborators. Network.

Join a conversation