Human pathology

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sensorineural hearing loss

sensorineural deafness

Etiology

- mutations in MYO1A coding for myosin-I (12736868)

References

- Schrijver I. Hereditary non-syndromic sensorineural hearing loss: transforming silence to sound. J Mol Diagn. 2004 Nov;6(4):275-84. PMID: 15507665