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1  题目：Sequence analysis of the complete mitochondrial genome in patients with Leber's hereditary optic neuropathy lacking the three most common pathogenic DNA mutations
  杂志：Biochem Biophys Res Commun. 2002 Jul 12;295(2):342-7.
  作者：Fauser S, Luberichs J, Besch D, Leo-Kottler B.

2  题目：Sequence analysis of Hungarian LHON patients not carrying the common primary mutations.
  杂志： J Inherit Metab Dis. 2002 Aug;25(4):323-4.
  作者：Horvath J, Horvath R, Karcagi V, Komoly S, Johns DR.

3  题目：Confirmation of the 14568 mutation in the mitochondrial ND6 gene as causative in Leber's hereditary optic neuropathy.
  杂志：Ophthalmic Genetics 23(3):191-197.
  作者：Fauser, S., Leo-Kottler, B., Besch, D. and Luberichs, J.

4 题目：Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russion LHON families.
   杂志：Human Genetics 109(1):33-39.
  作者：Brown, M. D., Zhadanov, S., Allen, J. C., Hosseini, S., Newman, N. J., Atamonov, V. V., Mikhailovskaya, I. E., Sukernik, R. I. and Wallace, D. C.

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Sequence analysis of the complete mitochondrial genome in patients with Leber's hereditary optic neuropathy lacking the three most common pathogenic DNA mutations

http://www.namipan.com/d/75ab4498c9d22267b09513e92f55254f52e081944e390100

Sequence analysis of Hungarian LHON patients not carrying the common primary mutations

Confirmation of the 14568 mutation in the
mitochondrial ND6 gene as causative in
Leber’s hereditary optic neuropathy

Novel mtDNA mutations and oxidative phosphorylation dysfunction in Russion LHON families

ok......

多谢小鹏8号帮忙，好神速啊，佩服中!