Loss-of-Function ENPP1 Mutations Cause Both Generalized Arterial Calcification of Infancy and Autosomal-Recessive Hypophosphatemic Rickets

✍ Scribed by Bettina Lorenz-Depiereux; Dirk Schnabel; Dov Tiosano; Gabriele Häusler; Tim M. Strom

• Book ID: 113422767
• Publisher: American Society of Human Genetics
• Year: 2010
• Tongue: English
• Weight: 285 KB
• Volume: 86
• Category: Article
• ISSN: 0002-9297
• DOI: 10.1016/j.ajhg.2010.01.006