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A Novel Missense Mutation (C84R) in a Patient with Type II Vitamin D-dependent Rickets

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Specialty Endocrinology
Date 2010 Feb 11
PMID 20146166
Citations 1
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Abstract

A 7-year-old boy with severe rickets that by clinical analysis was diagnosed as affected by type II vitamin D-dependent rickets, was evaluated for mutations in the vitamin D receptor gene (VDR). The molecular analysis showed a homozygous state for a novel missense mutation (C84R) in a highly conserved nucleotide in the second Zn finger of the DNA binding domain.

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Vitamin D receptor mutations in patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets.

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PMID: 24246681 PMC: 3933290. DOI: 10.1016/j.ymgme.2013.10.014.