Distinct Expression Patterns Of Causative Genes Responsible For Hereditary Progressive Hearing Loss In Non-Human Primate Cochlea
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/srep22250.pdf
Reference58 articles.
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3. Thoenes, M. et al. OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67). Orphanet J Rare Dis 10, 15, doi: 10.1186/s13023-015-0238-5 (2015).
4. Rost, S. et al. Novel form of X-linked nonsyndromic hearing loss with cochlear malformation caused by a mutation in the type IV collagen gene COL4A6. Eur J Hum Genet 22, 208–215, doi: 10.1038/ejhg.2013.108 (2014).
5. Plum, A. et al. Connexin31-deficiency in mice causes transient placental dysmorphogenesis but does not impair hearing and skin differentiation. Dev Biol 231, 334–347, doi: 10.1006/dbio.2000.0148 (2001).
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