Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencing. [electronic resource]
Producer: 20150206Description: 768-75 p. digitalISSN:- 1476-5438
- Arabs -- genetics
- Base Sequence
- Family Health
- Female
- Genetic Predisposition to Disease -- genetics
- Genomics -- methods
- Hearing Loss -- genetics
- High-Throughput Nucleotide Sequencing -- methods
- Humans
- Israel
- Jews -- genetics
- Male
- Mutation
- Myosin Heavy Chains -- genetics
- Myosin VIIa
- Myosins -- genetics
- Pedigree
- Phenotype
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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