Title
Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss
Author
Faculty/Department
Faculty of Pharmaceutical, Biomedical and Veterinary Sciences . Biomedical Sciences
Publication type
article
Publication
New York, N.Y. ,
Source (journal)
Human mutation. - New York, N.Y.
Volume/pages
11(1998) , p. 387-394
ISSN
1059-7794
ISI
000073299500006
Carrier
E
Target language
English (eng)
Full text (Publishers DOI)
Affiliation
University of Antwerp
E-info
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Handle