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Q36709030-5C265A99-14C8-452C-B44F-9ECB4178F234
Q36709030-5C265A99-14C8-452C-B44F-9ECB4178F234
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http://www.wikidata.org/entity/statement/Q36709030-5C265A99-14C8-452C-B44F-9ECB4178F234
Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3.
P2860
Q36709030-5C265A99-14C8-452C-B44F-9ECB4178F234
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36709030-5C265A99-14C8-452C-B44F-9ECB4178F234
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wasDerivedFrom
88eca0d440bdf5755a32c0c6cc6841a5fa51ff54
P2860
Characterization of GATA3 mutations in the hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome.