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Human Potassium Channel Subfamily K Member 7, KCNK7 ELISA Kit, 96T Cell Separation and Collection Mutations in COL18A1 are associated
Human Potassium Channel Subfamily K Member 7, KCNK7 ELISA Kit, 96T Cell Separation and Collection Mutations in COL18A1 are associated
Human Potassium Channel Subfamily K Member 7, KCNK7 ELISA Kit, 96T Cell Separation and Collection Mutations in COL18A1 are associated
Human Potassium Channel Subfamily K Member 7, KCNK7 ELISA Kit, 96T Cell Separation and Collection Mutations in COL18A1 are associated

Human Potassium Channel Subfamily K Member 7, KCNK7 ELISA Kit, 96T Cell Separation and Collection Mutations in COL18A1 are associated

SKU: 135735113

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PLN185.49 PLN223.49

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Human Potassium Channel Subfamily K Member 7, KCNK7 ELISA Kit, 96T Cell Separation and Collection Mutations in COL18A1 are associated

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Description

Mutations in COL18A1 are associated with Knobloch syndrome

Disruption of this gene negatively impacts mitochondrial and cytosolic iron homeostasis

many of which result from mutations in CFTR

and also interacts with other transcriptional regulators

but binds double-stranded RNA and DNA

Human Potassium Channel Subfamily K Member 7, KCNK7 ELISA Kit, 96T Cell Separation and Collection Mutations in COL18A1 are associated

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