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 A Johnson, E R Maher, R C Trembath

Research output: Contribution to journalArticlepeer-review

64 Citations (Scopus)
Original languageEnglish
Pages (from-to)443 - 448
Number of pages6
JournalJournal of Medical Genetics
Volume42
Issue number5
DOIs
Publication statusPublished - May 2005

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