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Q36087092-FDA1087B-04A2-4A1E-942D-BD76C612853C
Q36087092-FDA1087B-04A2-4A1E-942D-BD76C612853C
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http://www.wikidata.org/entity/statement/Q36087092-FDA1087B-04A2-4A1E-942D-BD76C612853C
A Homozygous [Cys25]PTH(1-84) Mutation That Impairs PTH/PTHrP Receptor Activation Defines a Novel Form of Hypoparathyroidism.
P2860
Q36087092-FDA1087B-04A2-4A1E-942D-BD76C612853C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36087092-FDA1087B-04A2-4A1E-942D-BD76C612853C
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wasDerivedFrom
de36aafe7f9c90d09c368679061b5b8d64832018
P2860
A new deletion ablating NESP55 causes loss of maternal imprint of A/B GNAS and autosomal dominant pseudohypoparathyroidism type Ib