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3. OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67)
作者：Michaela Thoenes (1)
Ulrike Zimmermann (2)
Inga Ebermann (1)
Martin Ptok (3)
Morag A Lewis (4)
Holger Thiele (5)
Susanne Morlot (6)
Markus M Hess (7)
Andreas Gal (8)
Tobias Eisenberger (9)
Carsten Bergmann (10) (9)
Gudrun N眉rnberg (5)
Peter N眉rnberg (11) (5)
Karen P Steel (4)
Marlies Knipper (2)
Hanno J枚rn Bolz (1) (9)

1. Institute of Human Genetics ; University Hospital of Cologne ; Cologne ; Germany
2. Molecular Physiology of Hearing ; Hearing Research Centre T眉bingen (THRC) ; Department of Otolaryngology ; University of T眉bingen ; T眉bingen ; Germany
3. Department of Phoniatrics and Pediatric Audiology ; Hannover Medical School ; Hannover ; Germany
4. Wolfson Centre for Age-Related Diseases ; King鈥檚 College London ; London ; UK
5. Cologne Center for Genomics (CCG) and Center for Molecular Medicine Cologne (CMMC) ; University of Cologne ; Cologne ; Germany
6. Institute for Human Genetics ; Hannover Medical School ; Hannover ; Germany
7. Department of Voice ; Speech and Hearing Disorders ; University Medical Center Hamburg-Eppendorf ; Hamburg ; Germany
8. Department of Human Genetics ; University Medical Center Hamburg-Eppendorf ; Hamburg ; Germany
9. Center for Human Genetics ; Bioscientia ; Ingelheim ; Germany
10. Renal Division ; Department of Medicine ; University Medical Center Freiburg ; Freiburg ; Germany
11. Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD) ; University of Cologne ; Cologne ; Germany
刊名：Orphanet Journal of Rare Diseases
出版年：2015
1
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