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HSPB3 Polyclonal Antibody, 50ul Plasmid Preparation PML is often involved in

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HSPB3 Polyclonal Antibody, 50ul Plasmid Preparation PML is often involved inThis gene encodes a muscle specific small heat shock protein. A mutation in this gene is the cause of autosomal dominant distal hereditary motor neuropathy type 2C.

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Description

PML is often involved in the translocation with the retinoic acid receptor alpha gene associated with acute promyelocytic leukemia (APL)

Mutations in HSD3B7 are associated with a congenital bile acid synthesis defect which leads to neonatal cholestasis

this protein may selectively affect the signaling process of ILK-mediated glycogen synthase kinase 3 beta (GSK3beta)

where it may be involved in the glycosylation of alpha-dystroglycan in skeletal muscle

Two transcript variants encoding distinct isofo

HSPB3 Polyclonal Antibody, 50ul Plasmid Preparation PML is often involved inThis gene encodes a muscle specific small heat shock protein. A mutation in this gene is the cause of autosomal dominant distal hereditary motor neuropathy type 2C.

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