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):

Published in:

Clinical Genetics (2017), Bd. 91, H. 6, S. 892-901

Verlagsangabe:

Wiley

Language:

English

Full text:

ISSN:

1399-0004

DDC Classifikation:

570 - Life sciences; biology
610 - Medicine and health

Dokumentart:

Article

This item appears in the following Collection(s)