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

SKU: 59559610076

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SEK185.49 SEK211.49

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

Store: avramcheva.com · Domain: avramcheva.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

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

Plays an important role in chromatin remodeling

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

Fibroblast growth factor 5 encoded by FGF5 is a member of the fibroblast growth factor (FGF) family

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

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