α-1-Antichymotrypsin gene A1252G variant (ACT Isehara-1) is associated with a lacunar type of ischemic cerebrovascular disease

Journal of Human Genetics

Volumn 46, Issue 1, 2001, Pages 45-47

  Tachikawa, H ^a   Tsuda, M ^a   Onoe, K ^a   Ueno, M ^a   Takagi, S ^a   Shinohara, Y ^a  

^a TOKAI UNIVERSITY   (Japan)

Author keywords

1 Antichymotrypsin; Ischemic cerebrovascular disease; Lacunar infarction; Plasma protease inhibitor; Risk factor of cerebrovascular disease; Serpine

Indexed keywords

ALPHA 1 ANTICHYMOTRYPSIN;

ADULT; AGED; ARTICLE; BRAIN INFARCTION; BRAIN ISCHEMIA; CEREBROVASCULAR DISEASE; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HUMAN; JAPAN; MAJOR CLINICAL STUDY; MALE; RISK FACTOR;

ADULT; AGED; ALPHA 1-ANTICHYMOTRYPSIN; BRAIN ISCHEMIA; FEMALE; HUMANS; MALE; MIDDLE AGED; MUTATION;

EID: 0035117262     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100380170125     Document Type: Article

References (4)

1. Human proteinase inhibitors
2. Detection of a New mutant α-1-antichymotrypsin in patients with occlusive cerebrovascular disease
3. α-1-Antichymotrypsin variant detected by PCR-single strand conformation polymorphism (PCR-SSCP) and direct sequencing
4. Special report from the National Institute of Neurological Disorders and Stroke: Classification of cerebrovascular diseases III