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Human G Protein-activated Inward Rectifier Potassium Channel 3, KCNJ9 ELISA Kit, 96T Custom Peptide Synthesis Mutations in this gene have

Human G Protein-activated Inward Rectifier Potassium Channel 3, KCNJ9 ELISA Kit, 96T Custom Peptide Synthesis Mutations in this gene have

Name: Human G Protein-activated Inward Rectifier Potassium Channel 3, KCNJ9 ELISA Kit, 96T Custom Peptide Synthesis Mutations in this gene have
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Human G Protein-activated Inward Rectifier Potassium Channel 3, KCNJ9 ELISA Kit, 96T Custom Peptide Synthesis Mutations in this gene have

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Description

Mutations in this gene have been associated with the X-linked form of Opitz syndrome

Mutations in this gene may be associated with adult-onset sensorimotor neuropathy| pigmentary retinopathy| and adrenomyeloneuropathy due to defects in bile acid synthesis

Inhibits the Wnt/beta-catenin signaling pathway

miscellaneous:The EU sequence has the INV (3) allotypic marker| Ala-45 and Val-83

Human G Protein-activated Inward Rectifier Potassium Channel 3, KCNJ9 ELISA Kit, 96T Custom Peptide Synthesis Mutations in this gene have

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