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- Table of Contents
Information about Generalized Myotonia Of Thomsen: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Most recent studies have shown that Generalized Myotonia Of Thomsen shares some biological mechanisms with becker-generalized-myotonia, becker-muscular-dystrophy, channelopathies, dystrophy, epilepsy, hypertrophy, muscle-weakness, muscular-dystrophy, muscular-stiffness, myasthenias, myopathy, myotonia-congenita, myotonic-disorders, myotonic-dystrophy, neuromuscular-diseases, pain, periodic-paralysis-(finding), weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Generalized Myotonia Of Thomsen, and have been seen in publications frequently: Cell Proliferation, Flight, Localization, Muscle Atrophy, Muscle Contraction, Muscle Hypertrophy, Pathogenesis, Reflex, Relaxation Of Muscle, Transepithelial Transport, Transport
Quite a number of genes have been found to play important roles in Generalized Myotonia Of Thomsen, such as AKR1B1, BBS9, CALR, CLCN1, CST7, DMPK, GRIP1, HDAC9, LCT, PGD, PSMC4, RPS6, SCN4A, TRGV3. 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.
Cell Proliferation | Flight | Localization |
Muscle Atrophy | Muscle Contraction | Muscle Hypertrophy |
Pathogenesis | Reflex | Relaxation Of Muscle |
Transepithelial Transport | Transport |