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Q49895247-3A2886D9-29AD-41F8-8C86-99B97022D1E1
Q49895247-3A2886D9-29AD-41F8-8C86-99B97022D1E1
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http://www.wikidata.org/entity/statement/Q49895247-3A2886D9-29AD-41F8-8C86-99B97022D1E1
Mosaicism for GNAS methylation defects associated with pseudohypoparathyroidism type 1B arose in early post-zygotic phases.
P2860
Q49895247-3A2886D9-29AD-41F8-8C86-99B97022D1E1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49895247-3A2886D9-29AD-41F8-8C86-99B97022D1E1
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wasDerivedFrom
a225a4f262888fcd23041ec9e8b48cdd7823d3ed
P2860
A new deletion ablating NESP55 causes loss of maternal imprint of A/B GNAS and autosomal dominant pseudohypoparathyroidism type Ib