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

J. Horvath, R. Horvath, V. Karcagi, S. Komoly, D. R. Johns

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

We describe sequence analysis of the mitochondrial DNA of five Hungarian patients diagnosed with probable LHON, who do not carry any of the three primary point mutations. We report three novel mutations, one of which might have a pathogenic role.

Original languageEnglish
Pages (from-to)323-324
Number of pages2
JournalJournal of Inherited Metabolic Disease
Volume25
Issue number4
DOIs
Publication statusPublished - Aug 2002

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Mitochondrial DNA
Point Mutation
Sequence Analysis
Mutation

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics
  • Endocrinology

Cite this

Sequence analysis of Hungarian LHON patients not carrying the common primary mutations. / Horvath, J.; Horvath, R.; Karcagi, V.; Komoly, S.; Johns, D. R.

In: Journal of Inherited Metabolic Disease, Vol. 25, No. 4, 08.2002, p. 323-324.

Research output: Contribution to journalArticle

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