NOTCH3 gene mutations in subjects clinically suspected of CADASIL

Journal of the Neurological Sciences

Volumn 307, Issue 1-2, 2011, Pages 144-148

  Mosca, Lorena ^a   Marazzi, Raffaella ^a   Ciccone, Alfonso ^a   Santilli, Ignazio ^a   Bersano, Anna ^b   Sansone, Valeria ^b   Grosso, Enrico ^c   Mandrile, Giorgia ^c   Giachino, Daniela Francesca ^c   Adobbati, Laura ^b   Corengia, Elisabetta ^d   Agostoni, Elio ^e   Fiumani, Anna ^e   Gallone, Salvatore ^c   Scarpini, Elio ^b   Guidotti, Mario ^d   Sterzi, Roberto ^a   Ajmone, Clara ^a   Marocchi, Alessandro ^a   Penco, Silvana ^a  

^a OSPEDALE NIGUARDA CA GRANDA   (Italy)

^b UNIVERSITY OF MILAN   (Italy)

^c UNIVERSITY OF TURIN   (Italy)

^d VALDUCE HOSPITAL   (Italy)

^e A MANZONI HOSPITAL   (Italy)

Author keywords

CADASIL; Genetic counselling; Genetic variations; NOTCH3; Stroke

Indexed keywords

NOTCH3 RECEPTOR;

ADULT; AGED; ARTICLE; CADASIL; EXON; FEMALE; GENE; GENE MUTATION; GENETIC ASSOCIATION; GENETIC COUNSELING; GENETIC IDENTIFICATION; GENETIC SCREENING; GENETIC VARIABILITY; HUMAN; INTRON; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

ADULT; AGED; AMINO ACID SUBSTITUTION; CADASIL; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC VARIATION; HUMANS; ITALY; MALE; MIDDLE AGED; POINT MUTATION; PROTEIN STRUCTURE, TERTIARY; RECEPTORS, NOTCH; YOUNG ADULT;

EID: 79959822577     PISSN: 0022510X     EISSN: 18785883     Source Type: Journal    
DOI: 10.1016/j.jns.2011.04.019     Document Type: Article

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