Extension of the clinical and molecular phenotype of DIAPH1 -associated autosomal dominant hearing loss (DFNA1 )-Reference-Cited by-同舟云学术

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

Author:

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.¹⁴

Affiliation:

1. Bioscientia Center for Human Genetics; Ingelheim Germany

2. Department of Otorhinolaryngology, Head and Neck Surgery; University of Cologne; Cologne Germany

3. Molecular Physiology of Hearing, Hearing Research Centre Tübingen (THRC), Department of Otolaryngology; University of Tübingen; Tübingen Germany

4. Institute of Human Genetics; University Hospital of Cologne; Cologne Germany

5. Gemeinschaftspraxis für Phoniatrie; Pädaudiologie und Hals-Nasen-Ohrenheilkunde; Regensburg Germany

6. Kompetenzzentrum für Humangenetik; Gynäkologie und Laboratoriumsmedizin; Regensburg Germany

Funder

GEERS-Stiftung

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

Reference49 articles.

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