Novel human pathological mutations. Gene symbol: NOTCH3. Disease: CADASIL.

Human genetics

Volumn 122, Issue 5, 2007, Pages 558-

  Bianchi, Silvia ^a   Dotti, M T ^a   Perretti, A ^a   De Rosa, A ^a   Manganelli, F ^a   Federico, A ^a  

^a UNIVERSITY OF SIENA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

NOTCH RECEPTOR; NOTCH3 PROTEIN, HUMAN; UNCLASSIFIED DRUG;

AMINO ACID SUBSTITUTION; ARTICLE; CADASIL; CODON; FEMALE; GENETICS; HUMAN; METABOLISM; MIDDLE AGED; MISSENSE MUTATION; ADULT; EXON; MALE; PEDIGREE; PHENOTYPE;

AMINO ACID SUBSTITUTION; CADASIL; CODON; FEMALE; HUMANS; MIDDLE AGED; MUTATION, MISSENSE; RECEPTORS, NOTCH; ADULT; EXONS; MALE; PEDIGREE; PHENOTYPE;

EID: 42049095940     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)