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FA8A Rabbit Polyclonal Antibody, 50ul[BT-AP02609] Electronic Pipette Mutations in this gene are

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FA8A Rabbit Polyclonal Antibody, 50ul[BT-AP02609] Electronic Pipette Mutations in this gene aredisease: Defects in F8 are the cause of hemophilia A (HEMA)

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Description

Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency

This gene encodes the beta subunit of the karyopherin receptor complex which interacts with nuclear localization signals to target nuclear proteins to the nucleus

in a region thought to be associated with susceptibility for psychiatric disorders and epilepsy

you'll be moving at lightning speed towards groundbreaking discoveries

Translocation t(11|19)(q21|p13) with MAML2

FA8A Rabbit Polyclonal Antibody, 50ul[BT-AP02609] Electronic Pipette Mutations in this gene aredisease: Defects in F8 are the cause of hemophilia A (HEMA)

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