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Article

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

29 Apr 2005

Abstract excerpt

This work was supported by a Wellcome Trust grant (programme grant\n062346/Z/00/Z, Functional Genomics National Autozygosity\nMapping Resource).

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Identifiers

PMID: 15863676
DOI: 10.1136/jmg.2004.026898

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