Congenital Deafness (Connexin 26)

TEST CODE MG01650
TEST NAME Congenital Deafness (Connexin 26)
RELATED GENE GJB2
SYNONYMOUS GJB2
OMIM 121011
HEREDITY Autosomal Dominant
CLINICAL AREA Congenital Deafness (Connexin 26) is a disease inherited as Autosomal Dominant. Mutations in the GJB2 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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