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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Bibliographische Detailangaben
Hauptverfasser: Coenen, Marieke J H, Tieleman, Alide A, Schijvenaars, Mascha M V A P, Leferink, Maike, Ranum, Laura P W, Scheffer, Hans, van Engelen, Baziel G M
Format: Artigo
Sprache:Inglês
Veröffentlicht: Nature Publishing Group 2011
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Article
Online Zugang: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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