Myotonic dystrophy CTG expansion affects synaptic vesicle proteins, neurotransmission and mouse behaviour

Myotonic dystrophy type 1 is a complex multisystemic inherited disorder, which displays multiple debilitating neurological manifestations. Despite recent progress in the understanding of the molecular pathogenesis of myotonic dystrophy type 1 in skeletal muscle and heart, the pathways affected in th...

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محفوظ في:
التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: Hernández-Hernández, Oscar, Guiraud-Dogan, Céline, Sicot, Géraldine, Huguet, Aline, Luilier, Sabrina, Steidl, Esther, Saenger, Stefanie, Marciniak, Elodie, Obriot, Hélène, Chevarin, Caroline, Nicole, Annie, Revillod, Lucile, Charizanis, Konstantinos, Lee, Kuang-Yung, Suzuki, Yasuhiro, Kimura, Takashi, Matsuura, Tohru, Cisneros, Bulmaro, Swanson, Maurice S., Trovero, Fabrice, Buisson, Bruno, Bizot, Jean-Charles, Hamon, Michel, Humez, Sandrine, Bassez, Guillaume, Metzger, Friedrich, Buée, Luc, Munnich, Arnold, Sergeant, Nicolas, Gourdon, Geneviève, Gomes-Pereira, Mário
التنسيق: Artigo
اللغة:Inglês
منشور في: Oxford University Press 2013
الموضوعات:
Original Articles
الوصول للمادة أونلاين:https://ncbi.nlm.nih.gov/pmc/articles/PMC3580270/
https://ncbi.nlm.nih.gov/pubmed/23404338
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/aws367
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