Abstract In the present study. we describe two novel cases of SCA5 with early onset. The first one. carrying a novel heterozygous de novo missense mutation in SPTBN2 gene. https://parisnaturalfoodes.shop/product-category/royal-jelly-honey/
Novel SPTBN2 gene mutation and first intragenic deletion in early onset spinocerebellar ataxia type 5
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