Dominantly inherited familial myasthenia gravis as a separate genetic entity without involvement of defined candidate gene loci.

F. Li, A. Szobor, R. Croxen, V. Anselmo, Q. P. Yuan, K. Lindblad, M. Schalling, S. Komoly, D. Beeson, C. Larsson

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Abstract

Myasthenia gravis (MG) is a sporadic autoimmune disorder affecting neuromuscular transmission. Very rarely autoimmune myasthenia gravis may be inherited within a family. We present here the genetic analysis of a Hungarian family where nine members from two generations are affected by myasthenia gravis. Genetic characterisation of this unique Hungarian family using linkage analysis and mutation screening excludes the involvement of defined candidate gene loci. These findings point to familial MG as a separate genetic entity. Identification of the underlying genetic defect in this family may greatly enhance our understanding of the pathogenesis of myasthenia gravis.

Original languageEnglish
Pages (from-to)289-294
Number of pages6
JournalInternational journal of molecular medicine
Volume7
Issue number3
Publication statusPublished - Mar 2001

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ASJC Scopus subject areas

  • Genetics

Cite this

Li, F., Szobor, A., Croxen, R., Anselmo, V., Yuan, Q. P., Lindblad, K., Schalling, M., Komoly, S., Beeson, D., & Larsson, C. (2001). Dominantly inherited familial myasthenia gravis as a separate genetic entity without involvement of defined candidate gene loci. International journal of molecular medicine, 7(3), 289-294.