Association of common genetic variants with vitamin D status in Malaysian children with epilepsy
Purpose: Children with epilepsy (CWE) are at risk of vitamin D deficiency. Single nucleotide polymorphisms (SNPs) affecting the vitamin D pathway are potentially important risk factors for serum 25-hydroxyvitamin D 25(OH)D] concentration. The aims of our study were to evaluate the association of vit...
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Main Authors: | , , , , , , , |
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Format: | Article |
Published: |
W.B. Saunders Ltd
2020
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Subjects: | |
Online Access: | http://eprints.um.edu.my/36582/ |
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