Single nucleotide polymorphisms of tissue inhibitor of metalloproteinase genes in familial moyamoya disease [6]

Neurosurgery

Volumn 60, Issue 3, 2007, Pages

  Kang, Hyun Seung ^a   Kim, Seung Ki ^a   Wang, Kyu Chang ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

TISSUE INHIBITOR OF METALLOPROTEINASE 2;

CLINICAL FEATURE; ETHNIC DIFFERENCE; GENE LOCUS; GENOTYPE; HETEROZYGOSITY; HUMAN; JAPAN; KOREA; LETTER; MOYAMOYA DISEASE; MULTIFACTORIAL INHERITANCE; PRIORITY JOURNAL; PROMOTER REGION; REVASCULARIZATION; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL SIGNIFICANCE;

EID: 33847419223     PISSN: 0148396X     EISSN: None     Source Type: Journal    
DOI: 10.1227/01.NEU.0000255366.19228.8D     Document Type: Letter

References (5)

1. Kang HS, Kim SK, Cho BK, Kim YY, Hwang YS, Wang KC: Single nucleotide polymorphisms of tissue inhibitor of metalloproteinase genes in familial moyamoya disease. Neurosurgery 58:1074-1080, 2006.
2. Ikeda H, Sasaki T, Yoshimoto T, Fukui M, Arinami T: Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26. Am J Hum Genet 64:533-537, 1999.
3. Inoue TK, Ikezaki K, Sasazuki T, Matsushima T, Fukui M: Linkage analysis of moyamoya disease on chromosome 6. J Child Neurol 15:179-182, 2000.
4. Sakurai K, Horiuchi Y, Ikeda H, Ikezaki K, Yoshimoto T, Fukui M, Arinami T: A novel susceptibility locus for moyamoya disease on chromosome 8q23. J Hum Genet 49:278-281, 2004.
5. Yamauchi T, Tada M, Houkin K, Tanaka T, Nakamura Y, Kuroda S, Abe H, Inoue T, Ikezaki K, Matsushima T, Fukui M: Linkage of familial moyamoya disease (spontaneous occlusion of the circle of Willis) to chromosome 17q25. Stroke 31:930-935, 2000.