A missense HTRA1 mutation expands CARASIL syndrome to the Caucasian population
- 30 November 2010
- journal article
- case report
- Published by Ovid Technologies (Wolters Kluwer Health) in Neurology
- Vol. 75 (22), 2033-2035
- https://doi.org/10.1212/wnl.0b013e3181ff96ac
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- A method and server for predicting damaging missense mutationsNature Methods, 2010
- A Chinese pedigree of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL): Clinical and radiological featuresJournal of Clinical Neuroscience, 2009
- Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel DiseaseThe New England Journal of Medicine, 2009
- Extensive loss of arterial medial smooth muscle cells and mural extracellular matrix in cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL)Neuropathology, 2007
- Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathyNeurology, 2002
- Familial Young-Adult-Onset Arteriosclerotic Leukoencephalopathy with Alopecia and Lumbago without Arterial HypertensionEuropean Neurology, 1995