Baylor College of Medicine: Novel Approach Reduces SCA1 Symptoms in Animal Model
HOUSTON, Texas, Aug. 11 -- The Baylor College of Medicine issued the following news release:
Research has shown that a mutation in the ATAXIN-1 gene leads to accumulation of Ataxin-1 (ATXN1) protein in brain cells and is the root cause of a rare genetic neurodegenerative disease known as spinocerebellar ataxia type 1 (SCA1). How healthy cells maintain a precise level of ATXN1 has remained a mystery, but now a study led by researchers at Baylor College of Medicine and the Jan and Dan . . .
Research has shown that a mutation in the ATAXIN-1 gene leads to accumulation of Ataxin-1 (ATXN1) protein in brain cells and is the root cause of a rare genetic neurodegenerative disease known as spinocerebellar ataxia type 1 (SCA1). How healthy cells maintain a precise level of ATXN1 has remained a mystery, but now a study led by researchers at Baylor College of Medicine and the Jan and Dan . . .