< Back to previous page

Publication

EMQN best practice guidelines for diagnostic testing of mutations causing non-syndromic hearing impairment at the DFNB1 locus

Journal Contribution - Journal Article

Journal: European journal of human genetics

ISSN: 1018-4813

Volume: 21

Pages: 1325 - 1329

Publication year:2013

DOI: https://doi.org/10.1038/ejhg.2013.83
Handle: https://hdl.handle.net/10067/1407010151162165141
WoS Id: 000325861500026