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Disease Info Card
Spastic Paraplegia, Hereditary
Information about Spastic Paraplegia, Hereditary: 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 Spastic Paraplegia, Hereditary
Most recent studies have shown that Spastic Paraplegia, Hereditary shares some biological mechanisms with amyotrophic-lateral-sclerosis, ataxia, atrophy, muscle-spasticity, muscular-atrophy, nerve-degeneration, nervous-system-disorder, nervousness, neurodegenerative-disorders, paraparesis, paraparesis-spastic, paraplegia, peroneal-muscular-atrophy-with-pyramidal-features-autosomal-dominant, primary-lateral-sclerosis, sclerosis, spastic-paraplegia, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Spastic Paraplegia, Hereditary, and have been seen in publications frequently: Cell Adhesion, Cell Death, Cognition, Cytokinesis, Endocytosis, Intracellular Transport, Localization, Membrane Fusion, Microtubule Severing, Muscle Atrophy, Myelination, Oxidative Phosphorylation, Pathogenesis, Protein Transport, Reflex, Ribosome Assembly, Secretion, Secretory Pathway, Translation, Transport
Quite a number of genes have been found to play important roles in Spastic Paraplegia, Hereditary, such as AAAS, ALS2, APP, ATL1, BSCL2, HSP90B2P, HSPD1, KIF5A, L1CAM, NIPA1, PLP1, REEP1, SOD1, SPAST, SPG11, SPG21, SPG7, ZFYVE26. 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.