Mitochondrial Deafness
Author:
Publisher
Informa UK Limited
Subject
General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.3109/07853899709007472
Reference57 articles.
1. Genetic diseases of hearing
2. A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene
3. Defective myosin VIIA gene responsible for Usher syndrome type IB
4. Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B.
5. The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells
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