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Leber hereditary optic neuropathy--a disease with a known molecular basis but a mysterious mechanism of pathology.
J Appl Genet. 2003;44(4):529-38.
J Appl Genet. 2003.
PMID: 14617834
Review.
Heteroplasmy analysis in the Polish patients with 11778A mutation responsible for Leber hereditary optic neuropathy.
Mroczek-Tońska K, Ratajska D, Guillot C, Sasiadek M, Ambroziak A, Lubos L, Bartnik E.
Mroczek-Tońska K, et al.
Acta Biochim Pol. 2002;49(1):257-62.
Acta Biochim Pol. 2002.
PMID: 12136948
Free article.
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[A case or Leber hereditary optic neuropathy (LHON): differential diagnosis with post inflammatory atrophy of nerve II using the mtDNA analysis].
Lubos L, Wajgt A, Maciejowski M, Mroczek-Tońska K, Bartnik E, Dziekanowska D.
Lubos L, et al. Among authors: mroczek tonska k.
Neurol Neurochir Pol. 2003 Jan-Feb;37(1):229-34.
Neurol Neurochir Pol. 2003.
PMID: 12910843
Polish.
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[Leber's hereditary optic neuropathy (LHON) with mutation at G3460A and MS-like phenotype].
Jamrozik Z, Tutaj A, Piechowski-Jóźwiak B, Mroczek-Tońska K, Bartnik E, Kwieciński H.
Jamrozik Z, et al. Among authors: mroczek tonska k.
Neurol Neurochir Pol. 2003 May-Jun;37(3):713-20.
Neurol Neurochir Pol. 2003.
PMID: 14593764
Review.
Polish.
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