Novel human pathological mutations. Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).

Human genetics

Volumn 121, Issue 5, 2007, Pages 649-

  Ferreira, Susana ^a   Costa, Cristina ^a   Oliveira, João Paulo ^a  

^a University of Porto   (Portugal)

Author keywords

[No Author keywords available]

Indexed keywords

NOTCH RECEPTOR; NOTCH3 PROTEIN, HUMAN; UNCLASSIFIED DRUG;

ARTICLE; CADASIL; GENETICS; HUMAN; MUTATION;

CADASIL; HUMANS; MUTATION; RECEPTORS, NOTCH;

EID: 35148829452     PISSN: 03406717     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)