Literature DB >> 2233926

Improved molecular-genetic diagnosis of Leber's hereditary optic neuropathy.

D R Johns.   

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Year:  1990        PMID： 2233926

Source DB:  PubMed          Journal:  N Engl J Med        ISSN： 0028-4793            Impact factor:   91.245


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  5 in total

1.  Allelic mutations of the fourth subunit of NADH dehydrogenase are not pathogenetically important in 11778-negative Leber hereditary optic neuropathy.

Authors:  D R Johns
Journal:  Am J Hum Genet       Date:  1991-06       Impact factor: 11.025

2.  Pitfalls in the molecular genetic diagnosis of Leber hereditary optic neuropathy (LHON).

Authors:  D R Johns; M J Neufeld
Journal:  Am J Hum Genet       Date:  1993-10       Impact factor: 11.025

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

4.  Single-cell analysis of intercellular heteroplasmy of mtDNA in Leber hereditary optic neuropathy.

Authors:  Y Kobayashi; H Sharpe; N Brown
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

5.  Evidence against an X-linked locus close to DXS7 determining visual loss susceptibility in British and Italian families with Leber hereditary optic neuropathy.

Authors:  M G Sweeney; M B Davis; A Lashwood; M Brockington; A Toscano; A E Harding
Journal:  Am J Hum Genet       Date:  1992-10       Impact factor: 11.025
  5 in total

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