View in EDS HTML Full Text PDF Full Text

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

Saved in:
Bibliographic Details
Title: Extension of the clinical and molecular phenotype of DIAPH1-associated autosomal dominant hearing loss ( DFNA1).
Authors: Neuhaus, C.1, Lang‐Roth, R.2, Zimmermann, U.3, Heller, R.4, Eisenberger, T.1, Weikert, M.5, Markus, S.6, Knipper, M.2, Bolz, H.J.1,4 hanno.bolz@bioscientia.de
Source: Clinical Genetics. Jun2017, Vol. 91 Issue 6, p892-901. 11p. 2 Color Photographs, 2 Diagrams, 2 Charts, 1 Graph.
Database: Academic Search Ultimate
Full text is not displayed to guests.
Description
ISSN:00099163
DOI:10.1111/cge.12915