SCOPUS 정보 검색 플랫폼

Lancet

Volumn 356, Issue 9247, 2000, Pages 2068-2069

Increased risk of stroke in patients with the A12308G polymorphism in mitochondria

(3) Pulkes, T a Sweeney, M G a Hanna, M G a

a UNIVERSITY COLLEGE LONDON (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL RNA;

ARTICLE; CLINICAL ARTICLE; CLINICAL FEATURE; GENE FREQUENCY; GENE MUTATION; GENETIC COUNSELING; GENETIC POLYMORPHISM; HUMAN; MELAS SYNDROME; PHENOTYPE; PRIORITY JOURNAL; RISK FACTOR; STROKE;

EID: 0034676760 PISSN: 01406736 EISSN: None Source Type: Journal
DOI: 10.1016/S0140-6736(00)03408-5 Document Type: Article

Times cited : (52)

References (5)

1
- 0031895748
- A tRNA suppressor mutation in human mitochondria
- (1998) Nat Genet , vol.18 , pp. 350-353
- El Meziane, A.¹ Lehtinen, S.K.² Hance, N.³

2
- 0031593558
- Mitochondrial tRNALeu isoform in lung carcinoma cybrid cells containing the np 3243 mtDNA mutation
- (1998) Hum Mol Genet , vol.7 , pp. 2141-2147
- El Meziane, A.¹ Lehtinen, S.K.² Holt, J.T.³ Jacobs, H.T.⁴

3
- 0019423856
- Sequence and organization of the human mitochondrial genome
- (1981) Nature , vol.290 , pp. 457-465
- Anderson, S.¹ Bankier, A.T.² Barrell, B.G.³

4
- 0026603422
- Mutation in mitochondrial tRNA genes: Non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegia
- (1992) Nucleic Acids Res , vol.20 , pp. 679-682
- Van den Ouweland, J.M.¹ Bruining, G.J.² Lindhout, D.³ Wit, J.M.⁴ Veldhuyzen, B.F.⁵ Maassen, J.A.⁶

5
- 2442735162
- Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: A systematic analysis of predisposing mutations and allelic variation in the PRNP gene
- (1996) Hum Genet , vol.98 , pp. 259-264
- Windl, O.¹ Dempster, M.² Estibeiro, J.P.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.