ArticleOrphanet journal of rare diseases2026
Six novel SACS mutations expand the autosomal recessive spastic ataxia of Charlevoix-Saguenay spectrum.
Susumu Ikenoshita et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
ArticleOrphanet journal of rare diseases2026
Susumu Ikenoshita et al.PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.