Spinocerebellar ataxia 4 is a devastating progressive movement disease that can begin as early as the late teens. Now, a multinational research team has conclusively identified the genetic difference that causes the disease, bringing answers to families and opening the door to future treatments.
After 25 years, researchers uncover genetic cause of rare neurological disease." ScienceDaily. ScienceDaily, 29 April 2024. <www.sciencedaily.com
A new study reports the identification of a previously unknown genetic cause of a late-onset cerebellar ataxia, a discovery that will improve diagnosis and open new treatment avenues for this ... An international team of researchers has discovered a new genetic mutation that leads to childhood glaucoma, and in the process, uncovered a new mechanism for causing the disease. They hope their ...
A research team has identified a new function of a gene called huntingtin, a mutation of which underlies the progressive neurodegenerative disorder known as Huntington's Disease. Using genetic mouse ... New research has shed light on the origins of spinocerebellar ataxia type 7 and demonstrates effective new therapeutic pathways for SCA7 and the more than 40 other types of spinocerebellar ...Hey Dave, I've Got an Idea for You: What's the Potential of AI-Led Workshopping?
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