Source:http://linkedlifedata.com/resource/lhgdn/association:46926
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
Mutational analysis of the RSPO1 gene in a 46, XX woman with true hermaphroditism, palmoplantar keratoderma, congenital bilateral corneal opacities, onychodystrophy, and hearing impairment, is reported.
|
| lhgdn:mesh_code |
D007645
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |