Clinical presentation of the DFNA loci where causative genes have not yet been cloned. DFNA4, DFNA6/14, DFNA7, DFNA16, DFNA20 and DFNA21. [electronic resource]
- Advances in oto-rhino-laryngology 2002
- 98-106 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
0065-3071
10.1159/000066820 doi
Auditory Threshold Carrier Proteins--genetics Disease Progression Genetic Linkage Hearing Loss, Sensorineural--diagnosis Humans Membrane Proteins--genetics Molecular Motor Proteins Mutation Myosin Heavy Chains--genetics Myosin Type II Phenotype