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    Identification of a novel mutation disrupting the DNA binding activity of GCM2 in autosomal recessive familial isolated hypoparathyroidism 
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    • Centre for Genomics and Child Health
    • Identification of a novel mutation disrupting the DNA binding activity of GCM2 in autosomal recessive familial isolated hypoparathyroidism
    •   QMRO Home
    • Blizard Institute
    • Centre for Genomics and Child Health
    • Identification of a novel mutation disrupting the DNA binding activity of GCM2 in autosomal recessive familial isolated hypoparathyroidism
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    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
    Show full item record
    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
    Collections
    • Centre for Genomics and Child Health [778]
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