The role of DMP1 in autosomal recessive hypophosphatemic rickets

J Musculoskelet Neuronal Interact. 2007 Oct-Dec;7(4):310-2.
No abstract available

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bone Development / genetics
  • Bone and Bones / metabolism*
  • Bone and Bones / physiopathology
  • Calcification, Physiologic / genetics
  • Cell Line
  • Chromosome Disorders / genetics
  • Chromosome Disorders / metabolism
  • Codon, Terminator / genetics
  • DNA Mutational Analysis
  • Extracellular Matrix Proteins / genetics*
  • Familial Hypophosphatemic Rickets / genetics*
  • Familial Hypophosphatemic Rickets / metabolism*
  • Familial Hypophosphatemic Rickets / physiopathology
  • Female
  • Frameshift Mutation / genetics
  • Genes, Recessive / genetics*
  • Genetic Predisposition to Disease / genetics*
  • Genetic Testing
  • Humans
  • Male
  • Peptides / genetics
  • Phosphoproteins / genetics*
  • Protein Structure, Tertiary / genetics

Substances

  • Codon, Terminator
  • DMP1 protein, human
  • Extracellular Matrix Proteins
  • Peptides
  • Phosphoproteins