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Q36442417-2BF590FE-B859-4691-A1C3-CF3434A350FD
Q36442417-2BF590FE-B859-4691-A1C3-CF3434A350FD
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Statement
http://www.wikidata.org/entity/statement/Q36442417-2BF590FE-B859-4691-A1C3-CF3434A350FD
De novo STX16 deletions: an infrequent cause of pseudohypoparathyroidism type Ib that should be excluded in sporadic cases.
P2860
Q36442417-2BF590FE-B859-4691-A1C3-CF3434A350FD
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36442417-2BF590FE-B859-4691-A1C3-CF3434A350FD
rank
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type
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wasDerivedFrom
bf433efd4a61d50481c88876f5b46ad8c8acb1d4
P2860
A new deletion ablating NESP55 causes loss of maternal imprint of A/B GNAS and autosomal dominant pseudohypoparathyroidism type Ib