Literature DB >> 8739946

Screening of mtDNA mutations in Italian LHON pedigrees.

C Carducci1, A M De Negri, V Leuzzi, C Terregino, M Torella, P Pivetti Pezzi, I Antonozzi.   

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Year:  1996        PMID： 8739946     DOI： 10.1007/bf01799410

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN： 0141-8955            Impact factor:   4.982


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  5 in total

1.  No genetic differences between affected and unaffected members of a German family with Leber's hereditary optic neuropathy (LHON) with respect to ten mtDNA point mutations associated with LHON.

Authors:  K D Gerbitz; A Paprotta; B Obermaier-Kusser; M Rietschel; K Zerres
Journal:  FEBS Lett       Date:  1992-12-21       Impact factor: 4.124

2.  Mitochondrial DNA mutation in an Italian family with Leber hereditary optic neuropathy.

Authors:  C Carducci; V Leuzzi; M Scuderi; A M De Negri; C B Gabrieli; I Antonozzi; A Pontecorvi
Journal:  Hum Genet       Date:  1991-10       Impact factor: 4.132

3.  Finger prick blood testing in Leber hereditary optic neuropathy.

Authors:  D Mackey; S Nasioulas; S Forrest
Journal:  Br J Ophthalmol       Date:  1993-05       Impact factor: 4.638

Review 4.  Molecular basis of mitochondrial DNA disease.

Authors:  M D Brown; D C Wallace
Journal:  J Bioenerg Biomembr       Date:  1994-06       Impact factor: 2.945

5.  Epidemic neuropathy in Cuba not associated with mitochondrial DNA mutations found in Leber's hereditary optic neuropathy patients. Cuba Neuropathy Field Investigation Team.

Authors:  N J Newman; A Torroni; M D Brown; M T Lott; M M Fernandez; D C Wallace
Journal:  Am J Ophthalmol       Date:  1994-08-15       Impact factor: 5.258
  5 in total

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