Homozygous C677T mutation of the 5,10 methylenetetrahydrofolate reductase gene and hyperhomocysteinemia in Italian patients with a history of early-onset ischemic stroke [5]

Stroke

Volumn 29, Issue 4, 1998, Pages 869-871

  Soriente, L ^a   Coppola, A ^a   Madonna, P ^a   Cerbone, A M ^a   Di Minno, G ^a   D'Angelo, A ^a  

^a UNIVERSITY OF NAPLES FEDERICO II   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL FEATURE; DISEASE ASSOCIATION; GENE MUTATION; GENETIC MARKER; GENOTYPE; HUMAN; HYPERHOMOCYSTEINEMIA; LETTER; MAJOR CLINICAL STUDY; PREVALENCE; PRIORITY JOURNAL; STROKE; TRANSIENT ISCHEMIC ATTACK;

EID: 0031922606     PISSN: 00392499     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.STR.29.4.869     Document Type: Letter

References (11)