Riboflavin Transporter Deficiency

TEST CODE MG04730
TEST NAME Riboflavin Transporter Deficiency
RELATED GENE SLC52A1
SYNONYMOUS SLC52A1
OMIM 615026
HEREDITY Autosomal Dominant
CLINICAL AREA Riboflavin Transporter Deficiency is an Autosomal Dominant inherited disease. Mutations in the SLC52A1 gene have been associated with the disease.
METHOD Next Generation Sequencing
SAMPLE TYPE Blood with EDTA
QUANTITY 3 mL
TAT 40 DAYS

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