Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets. [electronic resource]
Producer: 20091007Description: 1244-51 p. digitalISSN:- 1677-9487
- Alopecia -- drug therapy
- Base Sequence
- Calcitriol -- therapeutic use
- Child
- Familial Hypophosphatemic Rickets -- drug therapy
- Female
- Fibroblasts -- drug effects
- Humans
- Male
- Mutation
- RNA, Messenger -- genetics
- Receptors, Calcitriol -- genetics
- Sequence Analysis, DNA
- Steroid Hydroxylases -- genetics
- Vitamin D3 24-Hydroxylase
- Vitamins -- therapeutic use
- Young Adult
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Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
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