A New Deletion Ablating NESP55 Causes Loss of Maternal Imprint of A/B GNAS and Autosomal Dominant Pseudohypoparathyroidism Type Ib

✍ Scribed by Richard, N.; Abeguile, G.; Coudray, N.; Mittre, H.; Gruchy, N.; Andrieux, J.; Cathebras, P.; Kottler, M.-L.

• Book ID: 111893924
• Publisher: Endocrine Society
• Year: 2012
• Tongue: English
• Weight: 769 KB
• Volume: 97
• Category: Article
• ISSN: 0021-972X
• DOI: 10.1210/jc.2011-2804