CYP2R1 mutations causing vitamin D-deficiency rickets
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Clinical Biochemistry,Endocrinology,Molecular Biology,Molecular Medicine,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference32 articles.
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3. Clinical and molecular diagnosis of cerebrotendinous xanthomatosis with a review of the mutations in the CYP27A1 gene;Gallus;Neurol. Sci.,2006
4. Markedly reduced bile acid synthesis but maintained levels of cholesterol and vitamin D metabolites in mice with disrupted sterol 27-hydroxylase gene;Rosen;J. Biol. Chem.,1998
5. De-orphanization of cytochrome P450 2R1: a microsomal vitamin D 25-hydroxylase;Cheng;J. Biol. Chem.,2003
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