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Dutch myotonic dystrophy type 2 patients and a North-African DM2 family carry the common European founder haplotype
Myotonic dystrophy type 2 (DM2) is a progressive multisystem disease with muscle weakness and myotonia as main characteristics. The disease is caused by a repeat expansion in the zinc-finger protein 9 (ZNF9) gene on chromosome 3q21. Several reports show that patients from European ancestry share an...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2011
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3083617/ https://ncbi.nlm.nih.gov/pubmed/21224892 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2010.233 |
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