Notch3 mutations and the potential for diagnostic testing for CADASIL

Lancet

Volumn 350, Issue 9090, 1997, Pages 1490-

  Goate, A M ^a   Morris, J C ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTERY DISEASE; AUTOSOMAL DOMINANT DISORDER; BRAIN INFARCTION; DIAGNOSTIC TEST; GENE MUTATION; HUMAN; LEUKOENCEPHALOPATHY; PRIORITY JOURNAL; SHORT SURVEY;

EID: 0031590609     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(97)22047-7     Document Type: Note

References (5)

1. H Chabriat K Vahedi M Iba-Zizen Clinical spectrum of CADASIL: a study of 7 families Lancet 346 1995 934 939
2. E Tournier-Lasserve A Joutel J Melki Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome19ql2 Nat Genet 3 1993 256 259
3. A Joutel C Corpechot A Ducros Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia Nature 383 1996 707 710
4. S Artavanis-Tsakonas K Matsuno M Fortin Notch signaling Science 268 1995 225 232
5. RJ Greenspan The Notch gene, adhesion, and developmental fate in the Drosophila embryo New Biol 2 1990 595 600