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Q51014930-4E495298-6BAB-46DD-92F5-629213983511
Q51014930-4E495298-6BAB-46DD-92F5-629213983511
BestRank
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http://www.wikidata.org/entity/statement/Q51014930-4E495298-6BAB-46DD-92F5-629213983511
Simultaneous hyper- and hypomethylation at imprinted loci in a subset of patients with GNAS epimutations underlies a complex and different mechanism of multilocus methylation defect in pseudohypoparathyroidism type 1b.
P2860
Q51014930-4E495298-6BAB-46DD-92F5-629213983511
BestRank
Statement
http://www.wikidata.org/entity/statement/Q51014930-4E495298-6BAB-46DD-92F5-629213983511
rank
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wasDerivedFrom
314b90eb3282985e267d3326fd2612e8657ab819
P2860
A new deletion ablating NESP55 causes loss of maternal imprint of A/B GNAS and autosomal dominant pseudohypoparathyroidism type Ib