A case of Idiopathic Infantile Hypercalcaemia (IIH) persisting into adulthood, caused by compound heterozygous mutations of 1,25-dihydroxyvitamin D2 24-hydroxylase (CYP24A1)

Authors :: Victoria Stokes
Bahram Jafar-Mohammadi
Caroline M Gorvin
Rajesh Thakker
Fiona Ryan
Source :: Endocrine Abstracts.
Publication Year :: 2018
Publisher :: Bioscientifica, 2018.

Subjects :: medicine.medical_specialty
Endocrinology
CYP24A1
business.industry
Internal medicine
medicine
Infantile hypercalcaemia
Compound heterozygosity
business

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