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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

Store: jftbasic.com · Domain: jftbasic.com

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 encoded protein may play a role in endocytic trafficking

and CDK16/PCTAIRE1 as well as endocytosis associated proteins such as DNM1

which negatively regulates cell proliferation

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

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

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