Genomic organization of the human PEX gene mutated in X-linked dominant hypophosphatemic rickets

Genome Res. 1997 Jun;7(6):573-85. doi: 10.1101/gr.7.6.573.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cloning, Molecular
  • Codon, Nonsense
  • Exons
  • Female
  • Frameshift Mutation
  • Genetic Variation*
  • Humans
  • Hypophosphatemia, Familial / genetics*
  • Introns
  • Male
  • Molecular Sequence Data
  • Mutation*
  • Neprilysin / genetics
  • PHEX Phosphate Regulating Neutral Endopeptidase
  • Pedigree
  • Proteins / genetics*
  • Sequence Analysis, DNA
  • Sequence Deletion
  • Sequence Homology, Nucleic Acid

Substances

  • Codon, Nonsense
  • Proteins
  • PHEX Phosphate Regulating Neutral Endopeptidase
  • PHEX protein, human
  • Neprilysin

Associated data

  • GENBANK/AJ001637
  • GENBANK/Y08111
  • GENBANK/Y08112
  • GENBANK/Y08113
  • GENBANK/Y08114
  • GENBANK/Y08115
  • GENBANK/Y08116
  • GENBANK/Y08117
  • GENBANK/Y08118
  • GENBANK/Y08119
  • GENBANK/Y08120
  • GENBANK/Y08121
  • GENBANK/Y08122
  • GENBANK/Y08123
  • GENBANK/Y08124
  • GENBANK/Y08125
  • GENBANK/Y08126
  • GENBANK/Y08127
  • GENBANK/Y08128
  • GENBANK/Y08129
  • GENBANK/Y08130
  • GENBANK/Y08131
  • GENBANK/Y08132
  • GENBANK/Y10196