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Human Pancreatic Prohormone, PROPPY ELISA Kit, 96T Stepper Mutations in NECTIN4 are the

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Human Pancreatic Prohormone, PROPPY ELISA Kit, 96T Stepper Mutations in NECTIN4 are the

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Description

Mutations in NECTIN4 are the cause of ectodermal dysplasia-syndactyly syndrome type 1

This protein is involved in stimulating Wnt signaling pathways such as the regulation of axon pathfinding

Inhibits the activity of NK cells thus preventing cell lysis

It is uncertain whether Met-1 or Met-2 is the initiator

Human Pancreatic Prohormone, PROPPY ELISA Kit, 96T Stepper Mutations in NECTIN4 are the

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