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Human Golgin Subfamily A Member 1, GOLGA1 ELISA Kit, 96T Cell Culture a progressive demyelination disease which

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Human Golgin Subfamily A Member 1, GOLGA1 ELISA Kit, 96T Cell Culture a progressive demyelination disease which

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Description

a progressive demyelination disease which results in a variety of neurological symptoms and ultimately death

which negatively regulates cell proliferation

High levels of expression of this gene have been observed in several B cell-derived lymphomas

and thus plays a role in the cell response to environmental stresses

Specific mutations in DYSF have been shown to cause autosomal recessive limb girdle muscular dystrophy type 2B (LGMD2B) as well as Miyoshi myopathy

Human Golgin Subfamily A Member 1, GOLGA1 ELISA Kit, 96T Cell Culture a progressive demyelination disease which

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