https://www.selleckchem.com/pr....oducts/scutellarin.h
Common mutations in BTD deficiencies were indentified. Associating them with phenotype-genotype data will assist clinicians in better genetic counselling and management in the future by implementing prevention programmes. Key Words Biotinidase deficiency, BTD gene, Newborn screening, Inherited metabolic disease, Newborn screening programme. Common mutations in BTD deficiencies were indentified. Associating them with phenotype-genotype data will assist clinicians in better genetic counselling and management in the future by implement
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