BPES Disease

TEST CODE MG06220
TEST NAME BPES Disease
RELATED GENE FOXL2
SYNONYMOUS FOXL2
OMIM 110100
HEREDITY Autosomal Dominant, Autosomal Recessive
CLINICAL AREA BPES Disease is an autosomal dominant, autosomal recessive inherited disease. Mutations in the FOXL2 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