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Disease Info Card
Congenital Hypomyelinating Neuropathy
Information about Congenital Hypomyelinating Neuropathy: 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.
Overview of Congenital Hypomyelinating Neuropathy
Most recent studies have shown that Congenital Hypomyelinating Neuropathy shares some biological mechanisms with charcot-marie-tooth-disease, dejerine-sottas-disease-(disorder), demyelinating-diseases, demyelination, diseases-in-twins, hereditary-liability-to-pressure-palsies, hereditary-motor-and-sensory-neuropathies, inherited-neuropathy, muscle-hypotonia, nervousness, peripheral-neuropathy, polyneuropathy, reflex-abnormal, talipes-cavus, tissue-adhesions, tooth-diseases, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Hypomyelinating Neuropathy, and have been seen in publications frequently: Cell Cycle, Cell Death, Cell Dedifferentiation, Cell Differentiation, Cell Proliferation, Dedifferentiation, Innervation, Myelin Maintenance, Myelination, Pathogenesis, Regeneration, Regulation Of Myelination, Schwann Cell Differentiation, Schwann Cell Proliferation, Segmentation, Translation
Quite a number of genes have been found to play important roles in Congenital Hypomyelinating Neuropathy, such as CHN1, EGR2, GDAP1, GDI1, GJB1, KIF1B, LITAF, MAD2L1BP, MFN2, MPZ, MTMR2, NAB1, NAB2, NEFL, NR0B1, NR4A3, PES1, PMP22, PXMP2, RPLP0. 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.