Identification of a novel mutation disrupting the DNA binding activity of GCM2 in autosomal recessive familial isolated hypoparathyroidism (Q24301159)

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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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    Identification of a novel mutation disrupting the DNA binding activity of GCM2 in autosomal recessive familial isolated hypoparathyroidism (English)
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    S Patel
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    P King
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    C A Johnson
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    E R Maher
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    R C Trembath
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    May 2005
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    42
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    443-8
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    5
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