Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL) is a rare, severe, and deadly genetic disorder characterized by damage to small blood vessels in the brain. The condition triggers strokes. It is caused by mutations that lead to a loss of function of the protease HTRA1.
Team explores strategies for correcting mutations that cause stroke retrieved 16 July 2024 from https://medicalxpress.com/news/2024-07-team-explores-strategies-mutations.html
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New approaches for repairing the function of mutated proteins that cause strokeCerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL) is a rare, severe, and deadly genetic disorder characterized by damage to small blood vessels in the brain and which triggers strokes.
Read more »