A novel heterozygous HTRA1 mutation in an Asian family with CADASIL-like disease - Alex - The Leukodystrophy Charity

Get support Donate

Cerebral Autosomal Dominant Arteriopathy with Subcortical infarcts and Leukoencephalopathy (CADASIL)

https://pubmed.ncbi.nlm.nih.gov/34951056/