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- NP609262.RAXlkX0BXn6VPlqDXgLg4-pWfLXVj1F6mU3s5VFx1QOo4130_assertion type Assertion NP609262.RAXlkX0BXn6VPlqDXgLg4-pWfLXVj1F6mU3s5VFx1QOo4130_head.
- NP609262.RAXlkX0BXn6VPlqDXgLg4-pWfLXVj1F6mU3s5VFx1QOo4130_assertion description "[These mutations, along with a previously published missense allele linked to autosomal dominant progressive hearing loss (DFNA22), provide an allelic spectrum that probes the relationship between myosin VI dysfunction and the resulting phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP609262.RAXlkX0BXn6VPlqDXgLg4-pWfLXVj1F6mU3s5VFx1QOo4130_provenance.
- NP609262.RAXlkX0BXn6VPlqDXgLg4-pWfLXVj1F6mU3s5VFx1QOo4130_assertion evidence source_evidence_literature NP609262.RAXlkX0BXn6VPlqDXgLg4-pWfLXVj1F6mU3s5VFx1QOo4130_provenance.
- NP609262.RAXlkX0BXn6VPlqDXgLg4-pWfLXVj1F6mU3s5VFx1QOo4130_assertion SIO_000772 12687499 NP609262.RAXlkX0BXn6VPlqDXgLg4-pWfLXVj1F6mU3s5VFx1QOo4130_provenance.
- NP609262.RAXlkX0BXn6VPlqDXgLg4-pWfLXVj1F6mU3s5VFx1QOo4130_assertion wasDerivedFrom befree-20140225 NP609262.RAXlkX0BXn6VPlqDXgLg4-pWfLXVj1F6mU3s5VFx1QOo4130_provenance.
- NP609262.RAXlkX0BXn6VPlqDXgLg4-pWfLXVj1F6mU3s5VFx1QOo4130_assertion wasGeneratedBy ECO_0000203 NP609262.RAXlkX0BXn6VPlqDXgLg4-pWfLXVj1F6mU3s5VFx1QOo4130_provenance.