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Volumn 67, Issue 9, 2010, Pages 1140-1143

POLG1 variations presenting as multiple sclerosis

Author keywords

[No Author keywords available]

Indexed keywords

BETA INTERFERON; CORTICOSTEROID; MITOCHONDRIAL DNA; OLIGOCLONAL BAND; DNA DIRECTED DNA POLYMERASE; POLG PROTEIN, HUMAN;

EID: 77957088238     PISSN: 00039942     EISSN: 15383687     Source Type: Journal    
DOI: 10.1001/archneurol.2010.219     Document Type: Article
Times cited : (35)

References (7)
  • 2
    • 57849140614 scopus 로고    scopus 로고
    • Molecular and clinical genetics of mitochondrial diseases due to POLG mutations
    • Wong L-JC, Naviaux RK, Brunetti-Pierri N, et al. Molecular and clinical genetics of mitochondrial diseases due to POLG mutations. Hum Mutat. 2008;29(9):E150-E172.
    • (2008) Hum Mutat , vol.29 , Issue.9
    • Wong, L.-J.C.1    Naviaux, R.K.2    Brunetti-Pierri, N.3
  • 3
    • 72449155684 scopus 로고    scopus 로고
    • The unfolding clinical spectrum of POLG mutations
    • Blok MJ, van den Bosch BJ, Jongen E, et al. The unfolding clinical spectrum of POLG mutations. J Med Genet. 2009;46(11):776-785.
    • (2009) J Med Genet , vol.46 , Issue.11 , pp. 776-785
    • Blok, M.J.1    Van Den Bosch, B.J.2    Jongen, E.3
  • 4
    • 17444424938 scopus 로고    scopus 로고
    • Clinically isolated syndromes suggestive of multiple sclerosis, part I: Natural history, pathogenesis, diagnosis, and prognosis
    • Miller D, Barkhof F, Montalban X, Thompson A, Filippi M. Clinically isolated syndromes suggestive of multiple sclerosis, part I: natural history, pathogenesis, diagnosis, and prognosis. Lancet Neurol. 2005;4(5):281-288.
    • (2005) Lancet Neurol , vol.4 , Issue.5 , pp. 281-288
    • Miller, D.1    Barkhof, F.2    Montalban, X.3    Thompson, A.4    Filippi, M.5
  • 5
    • 70349807756 scopus 로고    scopus 로고
    • Structural insight into processive human mitochondrial DNA synthesis and disease-related polymerase mutations
    • Lee YS, Kennedy WD, Yin YW. Structural insight into processive human mitochondrial DNA synthesis and disease-related polymerase mutations. Cell. 2009;139(2):312-324.
    • (2009) Cell , vol.139 , Issue.2 , pp. 312-324
    • Lee, Y.S.1    Kennedy, W.D.2    Yin, Y.W.3
  • 7
    • 0026782507 scopus 로고
    • Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation
    • Harding AE, Sweeney MG, Miller DH, et al. Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation. Brain. 1992;115(pt 4):979-989.
    • (1992) Brain , vol.115 , Issue.PART 4 , pp. 979-989
    • Harding, A.E.1    Sweeney, M.G.2    Miller, D.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.