Skip to main content
Journal of Medical Genetics logoLink to Journal of Medical Genetics
letter
. 2005 May;42(5):443–448. doi: 10.1136/jmg.2004.026898

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

L Baumber, C Tufarelli, S Patel, P King, C Johnson, E Maher, R Trembath
PMCID: PMC1736051  PMID: 15863676

Full Text

The Full Text of this article is available as a PDF (215.9 KB).


Articles from Journal of Medical Genetics are provided here courtesy of BMJ Publishing Group

RESOURCES