Wang QK

Update on the molecular genetics of vascular anomalies.

Lymphat Res Biol 3:226-33 (2005)
DOI:10.1089/lrb.2005.3.226

Joutel A

Pathogenesis of CADASIL: transgenic and knock-out mice to probe function and dysfunction of the mutated gene, Notch3, in the cerebrovasculature.

Bioessays 33:73-80 (2011)
DOI:10.1002/bies.201000093

Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, Alamowitch S, Domenga V, Cecillion M, Marechal E, Maciazek J, Vayssiere C, Cruaud C, Cabanis EA, Ruchoux MM, Weissenbach J, Bach JF, Bousser MG, Tournier-Lasserve E

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia.

Nature 383:707-10 (1996)
DOI:10.1038/383707a0

Verdura E, Herve D, Scharrer E, Amador Mdel M, Guyant-Marechal L, Philippi A, Corlobe A, Bergametti F, Gazal S, Prieto-Morin C, Beaufort N, Le Bail B, Viakhireva I, Dichgans M, Chabriat H, Haffner C, Tournier-Lasserve E

Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel disease.

Brain 138:2347-58 (2015)
DOI:10.1093/brain/awv155