Related references
Note: Only part of the references are listed.Hypercalcemia, Hypercalciuria, and Elevated Calcitriol Concentrations with Autosomal Dominant Transmission Due to CYP24A1 Mutations: Effects of Ketoconazole Therapy
Peter J. Tebben et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2012)
Genetic Defect in CYP24A1, the Vitamin D 24-Hydroxylase Gene, in a Patient with Severe Infantile Hypercalcemia
Andrew Dauber et al.
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM (2012)
CYP24A1Mutations in Idiopathic Infantile Hypercalcemia
NEW ENGLAND JOURNAL OF MEDICINE (2011)
Mutations in CYP24A1 and Idiopathic Infantile Hypercalcemia
Karl P. Schlingmann et al.
NEW ENGLAND JOURNAL OF MEDICINE (2011)
Long-term follow-up of patients with idiopathic infantile hypercalcaemia
Jianping Huang et al.
PEDIATRIC NEPHROLOGY (2006)
Structural motif-based homology modeling of CYP27A1 and site-directed mutational analyses affecting vitamin D hydroxylation
DE Prosser et al.
BIOPHYSICAL JOURNAL (2006)
Altered pharmacokinetics of 1α,25-dihydroxyvitamin D3 and 25-hydroxyvitamin D3 in the blood and tissues of the 25-hydroxyvitamin D-24-hydroxylase (Cyp24a1) null mouse
S Masuda et al.
ENDOCRINOLOGY (2005)
Enzymes involved in the activation and inactivation of vitamin D
DE Prosser et al.
TRENDS IN BIOCHEMICAL SCIENCES (2004)
Share Paper
