Correlation between vitamin D receptor genetic polymorphism and 25-hydroxyvitamin D3 in vitamin D deficiency rickets

Chinese Journal of Contemporary Pediatrics

Volumn 12, Issue 7, 2010, Pages 544-546

  Gong, Yi Gu ^a   Li, Yu Ning ^a   Zhang, Wei Hua ^a   Liu, Li Jun ^a   Kang, Xi Guang ^a  

^a LANZHOU UNIVERSITY   (China)

Author keywords

25 Hydroxyvitamin D3; Child; Vitamin D deficiency rickets; Vitamin D receptor genetic polymorphism

Indexed keywords

CALCIFEDIOL; VITAMIN D RECEPTOR; CALCITRIOL RECEPTOR;

ALLELE; ARTICLE; CHILD; COMPARATIVE STUDY; CONTROLLED STUDY; ENZYME LINKED IMMUNOSORBENT ASSAY; FOK 1 GENE; GENE; GENE FREQUENCY; GENETIC ANALYSIS; GENETIC CORRELATION; GENETIC POLYMORPHISM; GENETIC SUSCEPTIBILITY; GENOTYPE; HEREDITY; HUMAN; INFANT; MAJOR CLINICAL STUDY; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; RECEPTOR GENE; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; RICKETS; VITAMIN BLOOD LEVEL; VITAMIN D DEFICIENCY; BLOOD; FEMALE; GENETIC PREDISPOSITION; GENETICS; MALE;

CALCIFEDIOL; CHILD, PRESCHOOL; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; INFANT; MALE; POLYMORPHISM, GENETIC; RECEPTORS, CALCITRIOL; RICKETS;

EID: 77955352509     PISSN: 10088830     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (10)

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2. Orton SM, Morris AP, Herrera BM, Ramagopalan SV, Lincoln MR, Chao MJ, et al. Evidence for genetic regulation of vitamin D status in twins with multiple sclerosis[J]. Am J Clin Nutr, 2008,88(2):441447.
3. Smolders J, Damoiseaux J, Menheere P, Cohen Tervaert JW, Hupperts R. Fok-I vitamin D receptor gene polymorphism (Rs10735810) and vitamin D metabolism in multiple sclerosis [J]. J Neuroimmunol, 2009,207(1-2):117-121.