Format

Send to

Choose Destination
N Engl J Med. 2003 Apr 24;348(17):1664-70.

A mutation of PCDH15 among Ashkenazi Jews with the type 1 Usher syndrome.

Author information

1
Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, Md 20850, USA.
PMID:
12711741
DOI:
10.1056/NEJMoa021502
[Indexed for MEDLINE]
Free full text

Supplemental Content

Full text links

Icon for Atypon
Loading ...
Support Center