Paramyotonia Congenita (disorder)

Overview of Paramyotonia Congenita (disorder)

Most recent studies have shown that Paramyotonia Congenita (disorder) shares some biological mechanisms with cardiac-arrhythmia, channelopathies, cold-intolerance, dystrophy, familial-periodic-paralysis, hyperkalemic-periodic-paralysis, hypokalemic-periodic-paralysis, malignant-hyperpyrexia-due-to-anesthesia, malignant-paraganglionic-neoplasm, muscle-weakness, muscular-stiffness, myopathy, myotonia-congenita, myotonic-disorders, myotonic-dystrophy, neuromuscular-diseases, periodic-paralysis-(finding), weakness.

Among the many pathways, these few ones have gauged particular interests from scientists studying Paramyotonia Congenita (disorder), and have been seen in publications frequently: Aging, Glycolysis, Ion Transport, Membrane Depolarization, Membrane Repolarization, Muscle Contraction, Muscle Hypertrophy, Pathogenesis, Reflex, Relaxation Of Muscle, Response To Cold, Transport

Quite a number of genes have been found to play important roles in Paramyotonia Congenita (disorder), such as CACNA1S, CLCN1, CNBP, CST7, DBNL, DLC1, DMPK, HP, KCNE3, MYCBP2, PAM, PSMC1, PSMD3, RPS4X, RPS4Y1, SCN4A, SCN5A, SCN9A, SPTA1. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.

Paramyotonia Congenita (disorder) Related Genes

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Pathways Related to Paramyotonia Congenita (disorder)

This information is being compiled and will come in a future update

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