Distribution and Structure of DM2 Repeat Tract Alleles in the German Population

Autosomal dominant inherited Myotonic dystrophy type 1 and 2 (DM1 and DM2) are the most frequent muscle dystrophies in the European population and are caused by repeat expansion mutations. For Germany cumulative empiric evidence suggests an estimated prevalence of DM2 of roughly 9 in 100,000, theref...

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Detalles Bibliográficos
Autores principales: Mahyera, Alexis S., Schneider, Tamara, Halliger-Keller, Birgit, Schrooten, Katja, Hörner, Eva-Maria, Rost, Simone, Kress, Wolfram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6020772/
https://www.ncbi.nlm.nih.gov/pubmed/29973908
http://dx.doi.org/10.3389/fneur.2018.00463

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6020772/
https://www.ncbi.nlm.nih.gov/pubmed/29973908
http://dx.doi.org/10.3389/fneur.2018.00463

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