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Q38248966-5D0F3C99-771E-4854-811C-50672EEFEB2B
Q38248966-5D0F3C99-771E-4854-811C-50672EEFEB2B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38248966-5D0F3C99-771E-4854-811C-50672EEFEB2B
GNAS mutations in Pseudohypoparathyroidism type 1a and related disorders.
P2860
Q38248966-5D0F3C99-771E-4854-811C-50672EEFEB2B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38248966-5D0F3C99-771E-4854-811C-50672EEFEB2B
rank
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Statement
wasDerivedFrom
57a9ac62be4582fe3b49b20bf05a832e66828e7c
P2860
A new deletion ablating NESP55 causes loss of maternal imprint of A/B GNAS and autosomal dominant pseudohypoparathyroidism type Ib