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Human Potassium Channel Subfamily K Member 7, KCNK7 ELISA Kit, 96T Cell Separation and Collection The gene structure (number and
Human Potassium Channel Subfamily K Member 7, KCNK7 ELISA Kit, 96T Cell Separation and Collection The gene structure (number and
Human Potassium Channel Subfamily K Member 7, KCNK7 ELISA Kit, 96T Cell Separation and Collection The gene structure (number and
Human Potassium Channel Subfamily K Member 7, KCNK7 ELISA Kit, 96T Cell Separation and Collection The gene structure (number and

Human Potassium Channel Subfamily K Member 7, KCNK7 ELISA Kit, 96T Cell Separation and Collection The gene structure (number and

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Human Potassium Channel Subfamily K Member 7, KCNK7 ELISA Kit, 96T Cell Separation and Collection The gene structure (number and

Store: humanprojects.de · Domain: humanprojects.de

Description

The gene structure (number and length of exons) is similar among family members

Mutations in COL18A1 are associated with Knobloch syndrome

many of which result from mutations in CFTR

and also interacts with other transcriptional regulators

Inhibits TMPRSS7 (PubMed: 15853774)

Human Potassium Channel Subfamily K Member 7, KCNK7 ELISA Kit, 96T Cell Separation and Collection The gene structure (number and

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