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Disease Info Card
Apraxic Aphonia
Information about Apraxic Aphonia: 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 Apraxic Aphonia
Most recent studies have shown that Apraxic Aphonia shares some biological mechanisms with aphasia, aphasia-broca, apraxias, articulation-disorders, atrophy, brain-injuries, cerebral-infarction, cerebrovascular-accident, communication-impairment, dementia, developmental-disabilities, dysarthria, impairment-(finding), language-development-disorders, language-disorders, malnutrition, neurodegenerative-disorders, primary-progressive-aphasia-(disorder), progressive-aphasia, speech-disorders.
Among the many pathways, these few ones have gauged particular interests from scientists studying Apraxic Aphonia, and have been seen in publications frequently: Aging, Cognition, Localization, Muscle Atrophy, Sensory Processing, Short-term Memory, Translation, Visual Perception
Quite a number of genes have been found to play important roles in Apraxic Aphonia, such as BCAR1, CBS, CSE1L, CTNND1, ERC1, ETFA, FAS, FASN, FOXP2, GNL3, GRN, IFNG, LPA, MAPT, MUC1, RANGAP1, SLC17A5, SLC6A8. 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.
Pathways Related to Apraxic Aphonia
This information is being compiled and will come in a future update
| Aging | Cognition | Localization |
| Muscle Atrophy | Sensory Processing | Short term Memory |
| Translation | Visual Perception |