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A new deletion ablating NESP55 causes loss of maternal imprint of A/B GNAS and autosomal dominant pseudohypoparathyroidism type Ib |
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| Authors: | Richard Nicolas Abeguilé Genevieve Coudray Nadia Mittre Hervé Gruchy Nicolas Andrieux Joris Cathebras Pascal Kottler Marie-Laure |
| Affiliation: | Centre Hospitalier Universitaire (CHU) de Caen, Department of Genetics, Caen F-14033, France. |
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