Activating NOTCH3 mutation in a patient with small-vessel-disease of the brain.

Human mutation

Volumn 29, Issue 3, 2008, Pages 452-

  Fouillade, Charles ^a   Chabriat, Hugues ^a   Riant, Florence ^a   Mine, Manuèle ^a   Arnoud, Minh ^a   Magy, Laurent ^a   Bousser, Marie Germaine ^a   Tournier Lasserve, Elisabeth ^a   Joutel, Anne ^a  

^a INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

NOTCH RECEPTOR; NOTCH3 PROTEIN, HUMAN; RECOMBINANT PROTEIN; UNCLASSIFIED DRUG;

AMINO ACID SUBSTITUTION; ANIMAL; ARTICLE; CADASIL; CASE REPORT; CELL STRAIN 3T3; CHEMISTRY; DIMERIZATION; FEMALE; GENETIC TRANSFECTION; GENETICS; HETEROZYGOTE; HUMAN; METABOLISM; MIDDLE AGED; MISSENSE MUTATION; MOUSE; PATHOLOGY; PROTEIN QUATERNARY STRUCTURE;

AMINO ACID SUBSTITUTION; ANIMALS; CADASIL; DIMERIZATION; FEMALE; HETEROZYGOTE; HUMANS; MICE; MIDDLE AGED; MUTATION, MISSENSE; NIH 3T3 CELLS; PROTEIN STRUCTURE, QUATERNARY; RECEPTORS, NOTCH; RECOMBINANT PROTEINS; TRANSFECTION;

EID: 41449118736     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.9527     Document Type: Article

References (0)