spinocerebellar ataxia type 4Research
Recent research identifies the ATXN8OS intermediate expansion as a genetic modifier in spinocerebellar ataxia type 48. This discovery could enhance understanding of SCA48 and inform future therapeutic strategies.
atxn8os intermediate expansion acts as a genetic modifier in spinocerebellar ataxia type 48 sca48 stub1
Original title: “ATXN8OS Intermediate Expansion Acts as a Genetic Modifier in Spinocerebellar Ataxia Type 48 (SCA48/STUB1).”