A Novel Missense Mutation (C84R) in a Patient with Type II Vitamin D-dependent Rickets
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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.
Vitamin D receptor mutations in patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets.
J Malloy P, Tasic V, Taha D, Tutunculer F, Ying G, Yin L Mol Genet Metab. 2013; 111(1):33-40.
PMID: 24246681 PMC: 3933290. DOI: 10.1016/j.ymgme.2013.10.014.