Data di Pubblicazione:
2010
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.
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
Vitamine D receptor; Missense Mutation; Type II Vitamin D Dependent Rickets
Elenco autori:
Porcu, Loredana; Moi, Paolo; Cabriolu, Annalisa; Marini, MARIA GIUSEPPINA; Asunis, Isadora
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