De novo mutation in the NOTCH3 gene causing CADASIL
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) is one of the most common hereditary forms of stroke, and migraine with aura, mood disorders and dementia. CADASIL is caused by mutations of the NOTCH3 gene. This mutation is inherited as an autosoma...
|Main Authors:||, , , , , ,|
Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina
|Series:||Bosnian Journal of Basic Medical Sciences|