SCOPUS 정보 검색 플랫폼

Human Genetics

Volumn 105, Issue 5, 1999, Pages 513-514

Haplotypo-matched controls as a tool to discriminate polymorphisms from pathogenic mutations in mtDNA

(4) Lehtonen, Mervi S a Meinilä, Maria a Hassinen, Ilmo E a Majamaa, Kari a

a UNIVERSITY OF OULU (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ARTICLE; CHILDHOOD MORTALITY; CONTROLLED STUDY; DNA POLYMORPHISM; FEMALE; HAPLOTYPE; HUMAN; HUMAN CELL; INFANT; MAJOR CLINICAL STUDY; MALE; MORTALITY; MUTATION RATE; NEWBORN; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; RESTRICTION FRAGMENT; CASE CONTROL STUDY; COMPARATIVE STUDY; GENE FREQUENCY; GENETIC POLYMORPHISM; GENETICS; INFANT MORTALITY; MUTATION; POINT MUTATION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

CASE-CONTROL STUDIES; CHILD, PRESCHOOL; DNA, MITOCHONDRIAL; FEMALE; GENE FREQUENCY; HAPLOTYPES; HUMANS; INFANT; INFANT MORTALITY; INFANT, NEWBORN; MALE; MUTATION; POINT MUTATION; POLYMORPHISM, GENETIC; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH;

EID: 0032585955 PISSN: 03406717 EISSN: None Source Type: Journal
DOI: 10.1007/s004390051139 Document Type: Article

Times cited : (3)

References (7)

1
- 0032965396
- Mitochondrial DNA analysis: Polymorphism and pathogenicity
- Chinnery PF, Howell N, Andrews RM, Turnbull DM (1999) Mitochondrial DNA analysis: polymorphism and pathogenicity. J Med Genet 36:505-510
- (1999) J Med Genet , vol.36 , pp. 505-510
- Chinnery, P.F.¹ Howell, N.² Andrews, R.M.³ Turnbull, D.M.⁴

2
- 0029638664
- Mitochondrial DNA and disease
- Johns DR (1995) Mitochondrial DNA and disease. N Engl J Med 333:638-644
- (1995) N Engl J Med , vol.333 , pp. 638-644
- Johns, D.R.¹

3
- 0009600003
- Gaudeamus, Hämeenlinna
- Koskinen S, Martelin T, Notkola IL, Notkola V, Pitkänen K (1994) Suomen väestö. Gaudeamus, Hämeenlinna
- (1994) Suomen Väestö
- Koskinen, S.¹ Martelin, T.² Notkola, I.L.³ Notkola, V.⁴ Pitkänen, K.⁵

4
- 0029587469
- Molecular genetic aspects of human mitochondrial disorders
- Larsson N-G, Clayton DA (1995) Molecular genetic aspects of human mitochondrial disorders. Annu Rev Genet 29:151-178
- (1995) Annu Rev Genet , vol.29 , pp. 151-178
- Larsson, N.-G.¹ Clayton, D.A.²

5
- 0032231623
- Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: Prevalence of the mutation in an adult population
- Majamaa K, Moilanen JS, Uimonen S, Remes AM, Salmela PI, Kärppä M, Majamaa-Voltti KAM, Rusanen H, Sorri M, Peuhkurinen KJ, Hassinen IE (1998) Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population. Am J Hum Genet 63:447-454
- (1998) Am J Hum Genet , vol.63 , pp. 447-454
- Majamaa, K.¹ Moilanen, J.S.² Uimonen, S.³ Remes, A.M.⁴ Salmela, P.I.⁵ Kärppä, M.⁶ Majamaa-Voltti, K.A.M.⁷ Rusanen, H.⁸ Sorri, M.⁹ Peuhkurinen, K.J.¹⁰ Hassinen, I.E.¹¹

6
- 0030249144
- Novel mutation in the mitochondrial DNA tRNA glycine gene associated with sudden unexpected death
- Santorelli FM, Schlessel JS, Slonim AE, DiMauro S (1996) Novel mutation in the mitochondrial DNA tRNA glycine gene associated with sudden unexpected death. Pediatr Neurol 15:145-149
- (1996) Pediatr Neurol , vol.15 , pp. 145-149
- Santorelli, F.M.¹ Schlessel, J.S.² Slonim, A.E.³ DiMauro, S.⁴

7
- 0030468182
- Classification of European mtDNAs from an analysis of three European populations
- Torroni A, Huoponen K, Francalacci P, Petrozzi M, Morelli L, Scozzari R, Obinu D, Savontaus M-L, Wallace DC (1996) Classification of European mtDNAs from an analysis of three European populations. Genetics 144:1835-1850
- (1996) Genetics , vol.144 , pp. 1835-1850
- Torroni, A.¹ Huoponen, K.² Francalacci, P.³ Petrozzi, M.⁴ Morelli, L.⁵ Scozzari, R.⁶ Obinu, D.⁷ Savontaus, M.-L.⁸ Wallace, D.C.⁹

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.