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Q35126234-5CC8B505-F07D-4C7E-889C-827B3CEBF0B6
Q35126234-5CC8B505-F07D-4C7E-889C-827B3CEBF0B6
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Statement
http://www.wikidata.org/entity/statement/Q35126234-5CC8B505-F07D-4C7E-889C-827B3CEBF0B6
Mutations in pseudohypoparathyroidism 1a and pseudopseudohypoparathyroidism in ethnic Chinese.
P2860
Q35126234-5CC8B505-F07D-4C7E-889C-827B3CEBF0B6
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35126234-5CC8B505-F07D-4C7E-889C-827B3CEBF0B6
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type
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Statement
wasDerivedFrom
ccfcfa4d0835cd0653e838a3fa93b8b0b13ef14d
P2860
A new deletion ablating NESP55 causes loss of maternal imprint of A/B GNAS and autosomal dominant pseudohypoparathyroidism type Ib