Paper
Paper
Search...
Search ResearchHub...
Ctrl+K
New
Home
Browse
Earn
Fund
RH Journal
Notebook
Lists
Leaderboard
RSC
USD
Changelog
Terms
Privacy
Issues
Docs
Support
Foundation
About
Whole-exome sequencing identifies recessive WDR62 mutatio... | ResearchHub
Paper
Paper
Search...
Search ResearchHub...
Ctrl+K
New
Home
Browse
Earn
Fund
RH Journal
Notebook
Lists
Leaderboard
RSC
USD
Changelog
Terms
Privacy
Issues
Docs
Support
Foundation
About
Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations
0
Authors
Kaya Bilgüvar
32 more
Kaya Bilgüvar
•
Ali Ozturk
30 more
•
Murat Günel
Published
August 22, 2010
Paper
Conversation
0
Reviews
0
Bounties
0
Sign in to review
Share your thoughts on this paper...
Best
Supporters
Support the authors with ResearchCoin
Tip RSC
Journal
Nature
Topics
Biology
Neuroscience
Molecular Biology
Genetics
Mutation
Show all topics
DOI
10.1038/nature09327
Other Formats
PDF
Supporters
Support the authors with ResearchCoin
Tip RSC
Journal
Nature
Topics
Biology
Neuroscience
Molecular Biology
Genetics
Mutation
Show all topics
DOI
10.1038/nature09327
Other Formats
PDF
