OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67)

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OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67)

Author: Thoenes, Michaela; Zimmermann, Ulrike; Ebermann, Inga; Ptok, Martin; Lewis, Morag A.; Thiele, Holger; Morlot, Susanne; Hess, Markus M.; Gal, Andreas; Eisenberger, Tobias; Bergmann, Carsten; Nuernberg, Gudrun; Nuernberg, Peter; Steel, Karen P.; Knipper, Marlies; Bolz, Hanno Joern
Tübinger Autor(en):
Zimmermann, Ulrike
Knipper, Marlies
Published in: Orphanet Journal of Rare Diseases (2015), Bd. 10, Article 15
Verlagsangabe: Biomed Central Ltd
Language: English
Full text: http://dx.doi.org/10.1186/s13023-015-0238-5
ISSN: 1750-1172
DDC Classifikation: 570 - Life sciences; biology
610 - Medicine and health
Dokumentart: Article
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