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Human Potassium Channel Subfamily K Member 5, KCNK5 ELISA Kit, 96T Isothermal Amplification Mutations in this gene may

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Human Potassium Channel Subfamily K Member 5, KCNK5 ELISA Kit, 96T Isothermal Amplification Mutations in this gene may

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Description

Mutations in this gene may be associated with the common cavity phenotype

and modulate dopamine receptor D2-mediated events

Mutations in this gene are associated with Fuhrmann and Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndromes

Monothiol glutaredoxin involved in mitochondrial iron-sulfur (Fe/S) cluster transfer (PubMed: 20364084

but neither the silencing nor an expanded repeat region appear to manifest itself in a clear phenotypic manner

Human Potassium Channel Subfamily K Member 5, KCNK5 ELISA Kit, 96T Isothermal Amplification Mutations in this gene may

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