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A comparative study on riboflavin responsive multiple acyl-CoA dehydrogenation deficiency due to variants in FLAD1 and ETFDH gene
Results showed 65% of patients achieved clinical remission compared to 32% receiving standard therapy alone
That said, some people have trouble absorbing vitamin B12 from food and oral supplements and may need it in injectable form
tRNA methyltransferase homologous A gene mutation causes an autosomal-recessive genetic disorder commonly characterized by microcephaly, diabetes mellitus, and epilepsy
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