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Q47697488-993AA8EE-7343-4292-8241-3F3A8968CE4E
Q47697488-993AA8EE-7343-4292-8241-3F3A8968CE4E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47697488-993AA8EE-7343-4292-8241-3F3A8968CE4E
A novel deletion involving GNAS exon 1 causes PHP1A and further refines the region required for normal methylation at exon A/B.
P2860
Q47697488-993AA8EE-7343-4292-8241-3F3A8968CE4E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q47697488-993AA8EE-7343-4292-8241-3F3A8968CE4E
rank
NormalRank
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Statement
wasDerivedFrom
8c47215d99be70946be72be9a8c79ca7649c09c2
P2860
A new deletion ablating NESP55 causes loss of maternal imprint of A/B GNAS and autosomal dominant pseudohypoparathyroidism type Ib