Autosomal dominant pseudohypoparathyroidism type Ib: a novel inherited deletion ablating STX16 causes loss of imprinting at the A/B DMR.
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| Description | scientific article published on 17 January 2014 |
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author: Francesca M Elli Luisa de Sanctis Giovanna Mantovani Paolo Beck-Peccoz Gianmaria Miolo Anna Spada Erika Peverelli |
| Publication date | January 17, 2014 |
| Language | English |
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