Identification of a novel mutation disrupting the DNA binding activity of GCM2 in autosomal recessive familial isolated hypoparathyroidism

• L Baumber

Journal

• Journal of Medical Genetics

  Journal of Medical Genetics 42 (5), 443-448, 2005-05-01

  BMJ

Keywords

• Genetics (clinical)
• Genetics

Details

• CRID: 1361137046488102400
• NII Article ID: 30021655063
• DOI: 10.1136/jmg.2004.026898
• ISSN: 14686244
• Web Site: https://syndication.highwire.org/content/doi/10.1136/jmg.2004.026898
• Data Source:
  • Crossref
  • CiNii Articles