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Premutation allele pool in myotonic dystrophy type 2

BACKGROUND: The myotonic dystrophies (DM1, DM2) are the most common adult muscle diseases and are characterized by multisystem involvement. DM1 has been described in diverse populations, whereas DM2 seems to occur primarily in European Caucasians. Both are caused by the expression of expanded micros...

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Главные авторы: Bachinski, L L., Czernuszewicz, T, Ramagli, L S., Suominen, T, Shriver, M D., Udd, B, Siciliano, M J., Krahe, R
Формат: Artigo
Язык:Inglês
Опубликовано: American Academy of Neurology 2009
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC2677510/
https://ncbi.nlm.nih.gov/pubmed/19020295
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/01.wnl.0000333665.01888.33
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