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- Table of Contents
Information about Bulbar Palsy, Progressive, With Sensorineural Deafness: 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.
Most recent studies have shown that Bulbar Palsy, Progressive, With Sensorineural Deafness shares some biological mechanisms with amyotrophic-lateral-sclerosis, atrophy, bulbar-palsy-progressive, complete-hearing-loss, cranial-nerve-diseases, cranial-nerve-palsies, fazio-londe-syndrome, motor-neuron-disease, muscle-hypotonia, muscle-weakness, muscular-atrophy, nervous-system-disorder, neurodegenerative-disorders, primary-lateral-sclerosis, respiratory-failure, sclerosis, sensorineural-hearing-loss-(disorder), weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Bulbar Palsy, Progressive, With Sensorineural Deafness, and have been seen in publications frequently: Localization, Pathogenesis, Reflex, Riboflavin Transport, Translation, Transport
Quite a number of genes have been found to play important roles in Bulbar Palsy, Progressive, With Sensorineural Deafness, such as ACAT1, ETFDH, IGFALS, MADD, MTSS1, SLC52A1, SLC52A2, SLC52A3, SMN1, SNRPN, SOD1, TARDBP, UBQLN1, UBQLN2. 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.
Localization | Pathogenesis | Reflex |
Riboflavin Transport | Translation | Transport |