Literature DB >> 8280696

An atypical Leber's hereditary optic neuropathy with the 11778 mutation.

Y Hotta1, M Hayakawa, K Fujiki, K Shinohara, K Sado, A Kanai, K Yanashima.   

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Year:  1993        PMID： 8280696      PMCID： PMC504642          DOI： 10.1136/bjo.77.11.748

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN： 0007-1161            Impact factor:   4.638


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  6 in total

1.  The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.

Authors:  N J Newman; M T Lott; D C Wallace
Journal:  Am J Ophthalmol       Date:  1991-06-15       Impact factor: 5.258

2.  High frequency of mitochondrial ND4 gene mutation in Japanese pedigrees with Leber hereditary optic neuropathy.

Authors:  M Nakamura; F Ara; M Yamada; Y Hotta; M Hayakawa; K Fujiki; A Kanai; J Sakai; M Inoue; M Yamamoto
Journal:  Jpn J Ophthalmol       Date:  1992       Impact factor: 2.447

3.  Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.

Authors:  M D Brown; A S Voljavec; M T Lott; A Torroni; C C Yang; D C Wallace
Journal:  Genetics       Date:  1992-01       Impact factor: 4.562

4.  Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.

Authors:  D C Wallace; G Singh; M T Lott; J A Hodge; T G Schurr; A M Lezza; L J Elsas; E K Nikoskelainen
Journal:  Science       Date:  1988-12-09       Impact factor: 47.728

5.  A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy.

Authors:  K Huoponen; J Vilkki; P Aula; E K Nikoskelainen; M L Savontaus
Journal:  Am J Hum Genet       Date:  1991-06       Impact factor: 11.025

6.  Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation.

Authors:  N Howell; I Kubacka; M Xu; D A McCullough
Journal:  Am J Hum Genet       Date:  1991-05       Impact factor: 11.025
  6 in total
  2 in total

1.  Visual prognosis better in eyes with less severe reduction of visual acuity one year after onset of Leber hereditary optic neuropathy caused by the 11,778 mutation.

Authors:  Yukihiko Mashima; Kazuteru Kigasawa; Kei Shinoda; Masato Wakakura; Yoshihisa Oguchi
Journal:  BMC Ophthalmol       Date:  2017-10-18       Impact factor: 2.209

2.  Retinitis pigmentosa with optic neuropathy and COQ2 mutations: A case report.

Authors:  Kentaro Kurata; Katsuhiro Hosono; Masakazu Takayama; Masahisa Katsuno; Hirotomo Saitsu; Tsutomu Ogata; Yoshihiro Hotta
Journal:  Am J Ophthalmol Case Rep       Date:  2022-01-20
  2 in total

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