Concepedia

Publication | Open Access

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

DOIFull Paper Access

59

Citations

42

References

2015

Year

Michaela Thoenes, Ulrike Zimmermann, Inga Ebermann, M. Ptok, Morag A. Lewis, Hölger Thiele, Susanne Morlot, Andreas Gal, Tobias Eisenberger, Carsten Bergmann,
Orphanet Journal of Rare Diseases

References

YearCitations

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