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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)

Store: gaabil.dk · Domain: gaabil.dk

Description

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

The checkpoint kinase 2 encoded by CHEK2 is a cell cycle checkpoint regulator and putative tumor suppressor

Thr-54 protein is associated with increased fat oxidation and insulin resistance

a pseudogene may exist on chromosome 2

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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