Corneal Dystrophy Lattice Type 1

TEST CODE MG08960
TEST NAME Corneal Dystrophy Lattice Type 1
RELATED GENE LCD1
SYNONYMOUS LCD1
OMIM 122200
HEREDITY Autosomal Dominant
CLINICAL AREA Corneal Dystrophy Lattice Type 1 is an Autosomal Dominant inherited disease. Mutations in the LCD1 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