Charcot-marie-tooth Disease, Axonal, Type 2k

Overview of Charcot-marie-tooth Disease, Axonal, Type 2k

Most recent studies have shown that Charcot-marie-tooth Disease, Axonal, Type 2k shares some biological mechanisms with charcot-marie-tooth-disease, charcot-marie-tooth-disease-type-4a-(disorder), dysmyelopoietic-syndromes, external-ophthalmoplegia, flexed-fetal-attitude, hereditary-motor-and-sensory-neuropathies, inherited-neuropathy, leigh-disease, merrf-syndrome, mitochondrial-diseases, mitochondrial-neurogastrointestinal-encephalopathy-syndrome, neurodegenerative-disorders, neuropathy-ataxia-and-retinis-pigmentosa, ophthalmoplegia, polyneuropathy, scoliosis-unspecified.

Among the many pathways, these few ones have gauged particular interests from scientists studying Charcot-marie-tooth Disease, Axonal, Type 2k, and have been seen in publications frequently: Cell Cycle, Mitochondrial Fission, Mitosis, Transport

Quite a number of genes have been found to play important roles in Charcot-marie-tooth Disease, Axonal, Type 2k, such as ASXL1, FIS1, GDAP1, KIF1B, LMNA, MAD2L1BP, MFN2, PAFAH1B1, POLG, SF3B1, TUBB, TUBB2A, TYMP, YWHAE. 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.

Charcot-marie-tooth Disease, Axonal, Type 2k Related Genes

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Pathways Related to Charcot-marie-tooth Disease, Axonal, Type 2k

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

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