Mutations in KRIT1 in familial cerebral cavernous malformations

Neurosurgery

Volumn 46, Issue 5, 2000, Pages 1272-1279

  Zhang, Jun ^a   Clatterbuck, Richard E ^a   Rigamonti, Daniele ^a   Dietz, Harry C ^a  

^a JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Cerebral cavernous malformation; Genetic mutation; KRIT1

Indexed keywords

GLUTAMINE; MESSENGER RNA; OLIGONUCLEOTIDE;

AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BRAIN MALFORMATION; DNA SEQUENCE; ETHNIC GROUP; GENE AMPLIFICATION; GENE LOCUS; GENE MUTATION; GENETIC ANALYSIS; GENETIC LINKAGE; HUMAN; NORTHERN BLOTTING; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM;

EID: 0034061825     PISSN: 0148396X     EISSN: None     Source Type: Journal    
DOI: 10.1097/00006123-200005000-00064     Document Type: Article

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