Genetic predictors of celiac disease, lactose intolerance, and vitamin D function and presence of peptide morphins in urine of children with neurodevelopmental disorders. [electronic resource]
Producer: 20190306Description: 40-50 p. digitalISSN:- 1476-8305
- Case-Control Studies
- Celiac Disease -- blood
- Child
- Child, Preschool
- Female
- Genetic Variation
- Genotyping Techniques
- HLA-DQ Antigens -- metabolism
- Humans
- Lactose Intolerance -- blood
- Male
- Neurodevelopmental Disorders -- blood
- Peptides -- pharmacokinetics
- Receptors, Calcitriol -- blood
- Risk Factors
- Urinalysis
- Vitamin D -- blood
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Publication Type: Journal Article
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