ArticleNeurogenetics2025
A novel homozygous loss-of-function NOTCH3 variant in a Moroccan patient: expanding the spectrum beyond CADASIL.
Amal Ouskri et al.PubMed ↗Publisher ↗
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ArticleNeurogenetics2025
Amal Ouskri et al.PubMed ↗Publisher ↗
No numbers read from the abstract.