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Christiana K, George T, George F, Margarita T, Anna T, Costas F, Irene A
This analysis also found no statistically significant increase in risk (OR 1.39
Biotinidase Deficiency Profound biotinidase deficiency is an autosomal recessive disorder that is characterized by pathogenic variants in the BTD gene that result in enzyme activity that is less than 10% of the normal
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