Pontocerebellar Hypoplasia Type 1B

TEST CODE MG09580
TEST NAME Pontocerebellar Hypoplasia Type 1B
RELATED GENE EXOSC3
SYNONYMOUS EXOSC3
OMIM 614678
HEREDITY Autosomal Recessive
CLINICAL AREA Pontocerebellar Hypoplasia Type 1B is an autosomal recessively inherited disease. Mutations in the EXOSC3 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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