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Genetic Variation of the Vitamin D Binding Protein Affects Vitamin D Status and Response to Supplementation in Infants
Author(s) -
Maria Enlund-Cerullo,
Laura Koljonen,
Elisa HolmlundSuila,
Helena Hautaalus,
Jenni Rosendahl,
Saara Valkama,
Otto Helve,
Timo Hytinantti,
Heli Viljakainen,
Sture Andersson,
Outi Mäkitie,
Minna Pekkinen
Publication year - 2019
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.2019-00630
Subject(s) - vitamin d binding protein , vitamin d and neurology , single nucleotide polymorphism , vitamin d deficiency , haplotype , medicine , genotype , endocrinology , minor allele frequency , vitamin , biology , genetics , gene
Single nucleotide polymorphisms (SNPs) of the vitamin D binding protein encoding the GC (group component) gene affect 25-hydroxyvitamin D (25OHD) concentrations, but their influence on vitamin D status and response to vitamin D supplementation in infants is unknown.

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