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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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Bibliografische gegevens
Hoofdauteurs: Bachinski, L L., Czernuszewicz, T, Ramagli, L S., Suominen, T, Shriver, M D., Udd, B, Siciliano, M J., Krahe, R
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: American Academy of Neurology 2009
Onderwerpen:
Online toegang: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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