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Human Golgin Subfamily A Member 1, GOLGA1 ELISA Kit, 96T Cell Culture Specific mutations in DYSF have
Human Golgin Subfamily A Member 1, GOLGA1 ELISA Kit, 96T Cell Culture Specific mutations in DYSF have
Human Golgin Subfamily A Member 1, GOLGA1 ELISA Kit, 96T Cell Culture Specific mutations in DYSF have
Human Golgin Subfamily A Member 1, GOLGA1 ELISA Kit, 96T Cell Culture Specific mutations in DYSF have

Human Golgin Subfamily A Member 1, GOLGA1 ELISA Kit, 96T Cell Culture Specific mutations in DYSF have

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Human Golgin Subfamily A Member 1, GOLGA1 ELISA Kit, 96T Cell Culture Specific mutations in DYSF have

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Description

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

The protein encoded by LAIR2 (leukocyte associated immunoglobulin like receptor 2) is a member of the immunoglobulin superfamily

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

phosphoinositide degeneration

Human Golgin Subfamily A Member 1, GOLGA1 ELISA Kit, 96T Cell Culture Specific mutations in DYSF have

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