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Leber遗传性视神经病变30例临床分析 被引量:4

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出处 《中华眼底病杂志》 CAS CSCD 2004年第1期44-44,共1页 Chinese Journal of Ocular Fundus Diseases
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参考文献6

  • 1Yen MY,Wang AG,Chang WL,et al.Leber′s hereditary optic neuropathy-the spectrum of mitochondrial DNA mutations in Chinese patients.Jpn J Ophthalmol,2002,46:45-51.
  • 2Brown MD,Sun F,Wallace DC.Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484mutations on an mtDNA lineage.AmJ HumGenet,1997:60:381-387.
  • 3Nikoskelainen E,Hoyt W F,Nummelin K.Ophthalmoscopic findings in Leber's hereditary optic neuroretinopathy:the fundus findings in the affected family members.Arch Ophthalmol,1983,101:1059-1068.
  • 4Nikoskelainen E,Huoponen K,Juvonen V,et al.Ophthalmologic findings in Leber hereditary optic neuropathy with special reference to mtDNA mutations.Ophthalmology,1996,103:504-514.
  • 5Leo-Kottler B,Christ-Adler M.Leber optic neuropathy in women and children.Ophthalmologe,1999,96:698-701.
  • 6Hotta Y,Fujiki K,Hayakawa M,et al.Clinical features of Japanese Leber's hereditary optic neuropathy with 11778 mutation of mitochondrialDNA.JpnJ Ophthalmol,1995,39:96-108.

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