5-Oxoprolinase Deficiency

TEST CODE MG09350
TEST NAME 5-Oxoprolinase Deficiency
RELATED GENE OPLAH
SYNONYMOUS OPLAH
OMIM 614243
HEREDITY Autosomal Dominant/Autosomal Recessive
CLINICAL AREA 5-Oxoprolinase Deficiency is an autosomal recessive disease. Mutations in the OPLAH gene have been associated with the disease.
METHOD Next Generation Sequencing
SAMPLE TYPE Blood with EDTA
QUANTITY 3 ml
TAT 40 DAYS

ORDER OPTIONS AND PRICING

Discover genetic insights at your convenience. Contact Mikrogen anytime for information on order options, pricing, and comprehensive genetic testing services