Seven novel mutations in the PEX gene indicate molecular heterogeneity for X-linked hypophosphataemic rickets.

समान संसाधन

• X-linked hypophosphataemic rickets in a Saudi Arabian kindred results from a nonsense mutation of the PEX gene.
  द्वारा: Dixon, P, और अन्य
  प्रकाशित: (1997)
• Mutations of the PEX regulatory and C-terminal regions cause X-linked hypophosphataemia.
  द्वारा: Dixon, P, और अन्य
  प्रकाशित: (1997)
• X-linked hypophosphataemic rickets due to pseudo-exons of the PHEX gene.
  द्वारा: Christie, P, और अन्य
  प्रकाशित: (2000)
• Bridging markers defining the map position of X linked hypophosphataemic rickets.
  द्वारा: Thakker, R, और अन्य
  प्रकाशित: (1987)
• Mapping of human X-linked hypophosphataemic rickets by multilocus linkage analysis.
  द्वारा: Read, A, और अन्य
  प्रकाशित: (1986)