Source:http://linkedlifedata.com/resource/lhgdn/association:59651
Predicate | Object |
---|---|
lhgdn:found_in | |
lhgdn:geneRifSource |
identification of 6 heterozygous missense mutations in MYO1C and additional 5 heterozygous missense mutations in MYO1F in bilateral sensorineural hearing loss
|
lhgdn:mesh_code |
D006319
|
lhgdn:associationIdType | |
lhgdn:umls_code |