Reduced-penetrance Huntington’s disease-causing alleles with 39 CAG trinucleotide repeats could be a genetic factor of amyotrophic lateral sclerosis
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DOI: 10.1097/jcma.0000000000000837
Abstract: Background: Expanded HTT alleles with 40 or more CAG repeats were recently found to be a rare cause of frontotemporal dementia and amyotrophic lateral sclerosis (ALS) spectrum diseases. The aim of this study was to… read more here.
Keywords: htt; alleles cag; lateral sclerosis; cag repeats ... See more keywords