DMP1 mutations in autosomal recessive hypophosphatemia implicate a bone matrix protein in the regulation of phosphate homeostasis

Eitemau Tebyg

• Long-Term Clinical Outcome and Carrier Phenotype in Autosomal Recessive Hypophosphatemia Caused by a Novel DMP1 Mutation
  gan: Mäkitie, Outi, et al.
  Cyhoeddwyd: (2010)
• Identification of a Novel Dentin Matrix Protein-1 (DMP-1) Mutation and Dental Anomalies in a Kindred with Autosomal Recessive Hypophosphatemia
  gan: Turan, Serap, et al.
  Cyhoeddwyd: (2009)
• Molecular Analysis of DMP1 Mutants Causing Autosomal Recessive Hypophosphatemic Rickets
  gan: Farrow, Emily G., et al.
  Cyhoeddwyd: (2008)
• Recessive versus imprinted disorder: consanguinity can impede establishing the diagnosis of autosomal dominant pseudohypoparathyroidism type Ib
  gan: Turan, Serap, et al.
  Cyhoeddwyd: (2010)
• Loss-of-Function ENPP1 Mutations Cause Both Generalized Arterial Calcification of Infancy and Autosomal-Recessive Hypophosphatemic Rickets
  gan: Lorenz-Depiereux, Bettina, et al.
  Cyhoeddwyd: (2010)