Extension of the clinical and molecular phenotype of DIAPH1-associated autosomal dominant hearing loss (DFNA1)

DSpace Repository

Extension of the clinical and molecular phenotype of DIAPH1-associated autosomal dominant hearing loss (DFNA1)

Author: Neuhaus, C.; Lang-Roth, R.; Zimmermann, U.; Heller, R.; Eisenberger, T.; Weikert, M.; Markus, S.; Knipper, M.; Bolz, H. J.
Tübinger Autor(en):
Zimmermann, Ulrike
Published in: Clinical Genetics (2017), Bd. 91, H. 6, S. 892-901
Verlagsangabe: Wiley
Language: English
Full text: http://dx.doi.org/10.1111/cge.12915
ISSN: 1399-0004
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Article
Show full item record

This item appears in the following Collection(s)