Spectrum of genotype and clinical manifestations in cerebral cavernous malformations

Neurosurgery

Volumn 59, Issue 6, 2006, Pages 1278-1284

  Gault, Judith ^a   Sain, Stephan ^a   Hu, Ling Jia ^a   Awad, Issam A ^b  

^a UNIVERSITY OF COLORADO   (United States)

^b NORTHWESTERN UNIVERSITY   (United States)

Author keywords

Central nervous system; Cerebrovascular stroke; Genetics; Mutation; Vascular malformations

Indexed keywords

ARTICLE; BRAIN HEMORRHAGE; CCM1 GENE; CCM2 GENE; CCM3 GENE; CEREBRAL CAVERNOUS MALFORMATION; CLINICAL FEATURE; CONGENITAL BLOOD VESSEL MALFORMATION; CONTROLLED STUDY; FAMILIAL DISEASE; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC HETEROGENEITY; GENETIC VARIABILITY; GENOTYPE; GENOTYPE PHENOTYPE CORRELATION; HUMAN; HUMAN TISSUE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

ADULT; COLORADO; DNA MUTATIONAL ANALYSIS; FAMILY; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; GENOTYPE; HEMANGIOMA, CAVERNOUS, CENTRAL NERVOUS SYSTEM; HETEROZYGOTE; HUMANS; MALE; MICROTUBULE-ASSOCIATED PROTEINS; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; PREVALENCE; PROTO-ONCOGENE PROTEINS; RISK ASSESSMENT; RISK FACTORS;

EID: 33845617049     PISSN: 0148396X     EISSN: None     Source Type: Journal    
DOI: 10.1227/01.NEU.0000249188.38409.03     Document Type: Article

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