Peroneal Muscular Atrophy With Pyramidal Features, Autosomal Dominant

Overview of Peroneal Muscular Atrophy With Pyramidal Features, Autosomal Dominant

Most recent studies have shown that Peroneal Muscular Atrophy With Pyramidal Features, Autosomal Dominant shares some biological mechanisms with aortic-aneurysm-abdominal, ataxia, atrophy, dementia, haploinsufficiency, impaired-cognition, muscle-spasticity, neurodegenerative-disorders, paraparesis, paraparesis-spastic, paraplegia, peripheral-neuropathy, spastic-paraplegia, spastic-paraplegia-10-autosomal-dominant, spastic-paraplegia-hereditary, weakness.

Among the many pathways, these few ones have gauged particular interests from scientists studying Peroneal Muscular Atrophy With Pyramidal Features, Autosomal Dominant, and have been seen in publications frequently: Dna Modification, Localization, Membrane Fusion, Microtubule Severing, Pathogenesis, Secretory Pathway, Translation

Quite a number of genes have been found to play important roles in Peroneal Muscular Atrophy With Pyramidal Features, Autosomal Dominant, such as AAAS, APP, ATL1, CD38, CST7, EPHB1, GNL3L, HSP90B2P, KCNH8, KIF5A, NIPA1, PES1, REEP1, RTN2, SPAST, SPG7, TARDBP. 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.

Peroneal Muscular Atrophy With Pyramidal Features, Autosomal Dominant Related Genes

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Pathways Related to Peroneal Muscular Atrophy With Pyramidal Features, Autosomal Dominant

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

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