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

Volume
42
Pagination
443 - 448
DOI
10.1136/jmg.2004.026898
Journal
J MED GENET
Issue
5
ISSN
0022-2593
Metadata
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Authors
Baumber, L; Tufarelli, C; Patel, S; King, P; Johnson, CA; Maher, ER; Trembath, RC
URI
http://qmro.qmul.ac.uk/xmlui/handle/123456789/7513
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