TY  - GEN
AU  - Thomas,N J
AU  - Morris,C M
AU  - Scaravilli,F
AU  - Johansson,J
AU  - Rossor,M
AU  - De Lange,R
AU  - St Clair,D
AU  - Nicoll,J
AU  - Blank,C
AU  - Coulthard,A
AU  - Bushby,K
AU  - Ince,P G
AU  - Burn,D
AU  - Kalaria,R N
TI  - Hereditary vascular dementia linked to notch 3 mutations. CADASIL in British families
SN  - 0077-8923
PY  - 2000///0602
KW  - Cardiovascular Diseases
KW  - complications
KW  - Chromosomes, Human, Pair 19
KW  - Dementia, Multi-Infarct
KW  - genetics
KW  - Genetic Linkage
KW  - Humans
KW  - Mutation, Missense
KW  - Proto-Oncogene Proteins
KW  - Receptors, Cell Surface
KW  - Risk Factors
KW  - United Kingdom
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Review
UR  - https://doi.org/10.1111/j.1749-6632.2000.tb06379.x
ER  -