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Linkage of proximal myotonic myopathy to chromosome 3q.
Ricker, K; Grimm, T; Koch, M C; Schneider, C; Kress, W; Reimers, C D; Schulte-Mattler, W; Mueller-Myhsok, B; Toyka, K V; Mueller, C R.
Afiliação
  • Ricker K; Department of Neurology, University of Würzburg, Germany. Kenneth.Ricker@t-online.de
Neurology ; 52(1): 170-1, 1999 Jan 01.
Article em En | MEDLINE | ID: mdl-9921867
We performed genetic linkage analysis in nine German proximal myotonic myopathy (PROMM) families using DNA-markers D3S1541 and D3S1589 from the region of the recently discovered gene locus of myotonic dystrophy type 2 (DM2) on chromosome 3q. Two-point analysis supplied an lod score of 5.9. We conclude that a gene causing PROMM is located on chromosome 3q. PROMM and DM2 may be allelic disorders or may be caused by closely linked genes.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 3 / Ligação Genética / Miotonia Limite: Humans Idioma: En Ano de publicação: 1999 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 3 / Ligação Genética / Miotonia Limite: Humans Idioma: En Ano de publicação: 1999 Tipo de documento: Article