Spastic Paraplegia 10, Autosomal Dominant

Overview of Spastic Paraplegia 10, Autosomal Dominant

Most recent studies have shown that Spastic Paraplegia 10, Autosomal Dominant shares some biological mechanisms with aortic-aneurysm-abdominal, ataxia, dementia, dwarfism, hyperexplexia, muscle-spasticity, muscular-atrophy, neurodegenerative-disorders, paraparesis, paraplegia, peroneal-muscular-atrophy-with-pyramidal-features-autosomal-dominant, pyramidal-tract-dysfunction, scoliosis-unspecified, spastic-paraplegia, spastic-paraplegia-hereditary, trinucleotide-repeat-expansion, weakness.

Among the many pathways, these few ones have gauged particular interests from scientists studying Spastic Paraplegia 10, Autosomal Dominant, and have been seen in publications frequently: Chromosome Localization, Dna Modification, Localization, Pathogenesis

Quite a number of genes have been found to play important roles in Spastic Paraplegia 10, Autosomal Dominant, such as AAAS, APP, ATL1, ATXN1, ATXN2, ATXN3, GPHN, HSPB8, HSPD1, IFT81, KIF5A, NIPA1, REEP1, SAR1A, SLC30A6, SLC33A1, SPAST. 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.

Spastic Paraplegia 10, Autosomal Dominant Related Genes

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Pathways Related to Spastic Paraplegia 10, Autosomal Dominant

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

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