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
Usher Syndrome 1D and Nonsyndromic Autosomal Recessive De... | 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
Usher Syndrome 1D and Nonsyndromic Autosomal Recessive Deafness DFNB12 Are Caused by Allelic Mutations of the Novel Cadherin-Like Gene CDH23
0
Authors
Julie Bork
27 more
Julie Bork
•
Lin Peters
25 more
•
Robert Morell
Published
January 1, 2001
Paper
Conversation
0
Reviews
0
Bounties
0
Sign in to comment
Add a comment...
Best
Supporters
Support the authors with ResearchCoin
Tip RSC
Journal
The American Journal of Human Genetics
Topics
Biology
Sensory Systems
Molecular Biology
Mutation
Retinitis Pigmentosa
Show all topics
DOI
10.1086/316954
License
publisher-specific-oa
Supporters
Support the authors with ResearchCoin
Tip RSC
Journal
The American Journal of Human Genetics
Topics
Biology
Sensory Systems
Molecular Biology
Mutation
Retinitis Pigmentosa
Show all topics
DOI
10.1086/316954
License
publisher-specific-oa
