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Volumn 26, Issue 4, 2006, Pages 264-267

Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy

Author keywords

[No Author keywords available]

Indexed keywords

ADENINE NUCLEOTIDE; GUANINE NUCLEOTIDE; MITOCHONDRIAL DNA;

EID: 33751266872     PISSN: 10708022     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.wno.0000249318.88991.c4     Document Type: Article
Times cited : (19)

References (27)
  • 1
    • 34447600937 scopus 로고
    • Uber hereditare und congenital-angelegte Sehnervenleiden
    • Leber T. Uber hereditare und congenital-angelegte Sehnervenleiden. Graefe's Arch Ophthalmol 1871;17:249-91.
    • (1871) Graefe's Arch Ophthalmol , vol.17 , pp. 249-291
    • Leber, T.1
  • 2
    • 0023185081 scopus 로고
    • Leber's hereditary optic neuroretinopathy, a maternally inherited disease: A genealogic study in four pedigrees
    • Nikoskelainen EK, Savontaus ML, Wanne OP, et al. Leber's hereditary optic neuroretinopathy, a maternally inherited disease: a genealogic study in four pedigrees. Arch Ophthalmol 1987;105:665-71.
    • (1987) Arch Ophthalmol , vol.105 , pp. 665-671
    • Nikoskelainen, E.K.1    Savontaus, M.L.2    Wanne, O.P.3
  • 3
    • 0027180961 scopus 로고
    • Leber's hereditary optic neuropathy: New genetic considerations
    • Newman NJ. Leber's hereditary optic neuropathy: new genetic considerations. Arch Neurol 1993;50:540-8.
    • (1993) Arch Neurol , vol.50 , pp. 540-548
    • Newman, N.J.1
  • 4
    • 0024242545 scopus 로고
    • Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
    • Wallace DC, Singh G, Lott MT, et al. Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. Science 1988;242:1427-30.
    • (1988) Science , vol.242 , pp. 1427-1430
    • Wallace, D.C.1    Singh, G.2    Lott, M.T.3
  • 5
    • 0026757115 scopus 로고
    • An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy
    • Johns DR, Neufeld MJ, Park RD. An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy. Biochem Biophys Res Commun 1992;187:1551-7.
    • (1992) Biochem Biophys Res Commun , vol.187 , pp. 1551-1557
    • Johns, D.R.1    Neufeld, M.J.2    Park, R.D.3
  • 6
    • 0026746739 scopus 로고
    • Avariant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology
    • Mackey D, Howell N. Avariant of Leber hereditary optic neuropathy characterized by recovery of vision and by an unusual mitochondrial genetic etiology. Am J Hum Genet 1992;51:1218-28.
    • (1992) Am J Hum Genet , vol.51 , pp. 1218-1228
    • Mackey, D.1    Howell, N.2
  • 7
    • 0025897119 scopus 로고
    • Leber hereditary optic neuropathy: Involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation
    • Howell N, Kubacka I, Xu M, et al. Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation. Am J Hum Genet 1991;48:935-42.
    • (1991) Am J Hum Genet , vol.48 , pp. 935-942
    • Howell, N.1    Kubacka, I.2    Xu, M.3
  • 8
    • 0025910614 scopus 로고
    • A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy
    • Huoponen K, Vilkki J, Aula P, et al. A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy. Am J Hum Genet 1991;48:1147-53.
    • (1991) Am J Hum Genet , vol.48 , pp. 1147-1153
    • Huoponen, K.1    Vilkki, J.2    Aula, P.3
  • 9
    • 0029064615 scopus 로고
    • Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation
    • Harding AE, Sweeney MG, Govan GG, et al. Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation. Am J Hum Genet 1995;57:77-86.
    • (1995) Am J Hum Genet , vol.57 , pp. 77-86
    • Harding, A.E.1    Sweeney, M.G.2    Govan, G.G.3
  • 10
    • 0028945657 scopus 로고
    • Leber's hereditary optic neuropathy: The clinical relevance of different mitochondrial DNA mutations
    • Riordan-Eva P, Harding AE. Leber's hereditary optic neuropathy: the clinical relevance of different mitochondrial DNA mutations. J Med Genet 1995;32:81-7.
    • (1995) J Med Genet , vol.32 , pp. 81-87
    • Riordan-Eva, P.1    Harding, A.E.2
  • 11
    • 0031034482 scopus 로고    scopus 로고
    • Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage
    • Brown MD, Sun F, Wallace DC. Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage. Am J Hum Genet 1997;60:381-7.
    • (1997) Am J Hum Genet , vol.60 , pp. 381-387
    • Brown, M.D.1    Sun, F.2    Wallace, D.C.3
  • 12
    • 0036487995 scopus 로고    scopus 로고
    • The role of mtDNA background in disease expression: A new primary LHON mutation associated with Western Eurasian haplogroup
    • Brown MD, Starikovskaya E, Derbeneva O, et al. The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup. J Hum Genet 2002;110:130-8.
    • (2002) J Hum Genet , vol.110 , pp. 130-138
    • Brown, M.D.1    Starikovskaya, E.2    Derbeneva, O.3
  • 13
    • 0028928397 scopus 로고
    • Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees
    • Howell N, Kubacka I, Halvorson S, et al. Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees. Genetics 1995;140:285-302.
    • (1995) Genetics , vol.140 , pp. 285-302
    • Howell, N.1    Kubacka, I.2    Halvorson, S.3
  • 14
    • 16944363113 scopus 로고    scopus 로고
    • Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484
    • Torroni A, Petrozzi M, D'Urbano L, et al. Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484. Am J Hum Genet 1997;60:1107-21.
    • (1997) Am J Hum Genet , vol.60 , pp. 1107-1121
    • Torroni, A.1    Petrozzi, M.2    D'Urbano, L.3
  • 15
    • 2342540462 scopus 로고    scopus 로고
    • Mitochondrial DNA haplogroup distribution within Leber hereditary optic neuropathy pedigrees
    • Man PY, Howell N, Mackey DA, et al. Mitochondrial DNA haplogroup distribution within Leber hereditary optic neuropathy pedigrees. J Med Genet 2004;41:e41.
    • (2004) J Med Genet , vol.41
    • Man, P.Y.1    Howell, N.2    Mackey, D.A.3
  • 16
    • 33646448234 scopus 로고    scopus 로고
    • Mitochondrial genetics of mitochondrial diseases in Thailand
    • Lertrit P, Imsumran A, Trongpanich Y, et al. Mitochondrial genetics of mitochondrial diseases in Thailand. Siriraj Hosp Gaz 1998;50:53-64.
    • (1998) Siriraj Hosp Gaz , vol.50 , pp. 53-64
    • Lertrit, P.1    Imsumran, A.2    Trongpanich, Y.3
  • 17
    • 0026598898 scopus 로고
    • Southeast Asian mitochondrial DNA analysis reveals genetic continuity of ancient mongoloid migrations
    • Ballinger SW, Schurr TG, Torroni A, et al. Southeast Asian mitochondrial DNA analysis reveals genetic continuity of ancient mongoloid migrations. Genetics 1992;130:139-52.
    • (1992) Genetics , vol.130 , pp. 139-152
    • Ballinger, S.W.1    Schurr, T.G.2    Torroni, A.3
  • 18
    • 0035182136 scopus 로고    scopus 로고
    • The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy
    • Chinnery PF, Brown DT, Andrews RM, et al. The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy. Brain 2001;124:209-18.
    • (2001) Brain , vol.124 , pp. 209-218
    • Chinnery, P.F.1    Brown, D.T.2    Andrews, R.M.3
  • 19
    • 0030813676 scopus 로고    scopus 로고
    • Population genetics and disease susceptibility: Characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease
    • Hofmann S, Jaksch M, Bezold R, et al. Population genetics and disease susceptibility: characterization of central European haplogroups by mtDNA gene mutations, correlation with D loop variants and association with disease. Hum Mol Genet 1997;6:1835-46.
    • (1997) Hum Mol Genet , vol.6 , pp. 1835-1846
    • Hofmann, S.1    Jaksch, M.2    Bezold, R.3
  • 20
    • 0025225644 scopus 로고
    • Analysis of mitochondrial ND4 gene DNA sequence in Finnish families with Leber hereditary optic neuroretinopathy
    • Huoponen K, Vilkki J, Savontaus ML, et al. Analysis of mitochondrial ND4 gene DNA sequence in Finnish families with Leber hereditary optic neuroretinopathy. Genomics 1990;8:583-5.
    • (1990) Genomics , vol.8 , pp. 583-585
    • Huoponen, K.1    Vilkki, J.2    Savontaus, M.L.3
  • 21
    • 0032833421 scopus 로고    scopus 로고
    • Mitochondrial DNA variation in human evolution and disease
    • Wallace DC, Brown MD, Lott MT. Mitochondrial DNA variation in human evolution and disease. Gene 1999;238:211-30.
    • (1999) Gene , vol.238 , pp. 211-230
    • Wallace, D.C.1    Brown, M.D.2    Lott, M.T.3
  • 22
    • 0035070918 scopus 로고    scopus 로고
    • Mitochondrial DNA polymorphisms in Thailand
    • Fucharoen G, Fucharoen S, Horai S. Mitochondrial DNA polymorphisms in Thailand. J Hum Genet 2001;46:115-22.
    • (2001) J Hum Genet , vol.46 , pp. 115-122
    • Fucharoen, G.1    Fucharoen, S.2    Horai, S.3
  • 23
    • 0036023263 scopus 로고    scopus 로고
    • Mitochondrial DNA diversity in Southeast Asian populations
    • Schurr TG, Wallace DC. Mitochondrial DNA diversity in Southeast Asian populations. Hum Biol 2002;74:431-52.
    • (2002) Hum Biol , vol.74 , pp. 431-452
    • Schurr, T.G.1    Wallace, D.C.2
  • 25
    • 28144454984 scopus 로고    scopus 로고
    • Hudson G, Keers S, Yu Wai Man P, et al. Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder. Am J Hum Genet 2005;77:1086-91.
    • Hudson G, Keers S, Yu Wai Man P, et al. Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder. Am J Hum Genet 2005;77:1086-91.
  • 26
    • 0036947414 scopus 로고    scopus 로고
    • Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy
    • Sudoyo H, Suryadi H, Lertrit P, et al. Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy. J Hum Genet 2002;47:594-60.
    • (2002) J Hum Genet , vol.47 , pp. 594-560
    • Sudoyo, H.1    Suryadi, H.2    Lertrit, P.3
  • 27
    • 0041971164 scopus 로고    scopus 로고
    • Leber's hereditary optic neuropathy with 14484 mutation in Central Java, Indonesia
    • Nishioka T, Tasaki M, Soemantri A, et al. Leber's hereditary optic neuropathy with 14484 mutation in Central Java, Indonesia. J Hum Genet 2003;48:385-9.
    • (2003) J Hum Genet , vol.48 , pp. 385-389
    • Nishioka, T.1    Tasaki, M.2    Soemantri, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.