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The Neuromuscular Junction and Wide Heterogeneity of Congenital Myasthenic Syndromes

Congenital myasthenic syndromes (CMS) are genetic disorders characterised by impaired neuromuscular transmission. This review provides an overview on CMS and highlights recent advances in the field, including novel CMS causative genes and improved therapeutic strategies. CMS due to mutations in SLC5...

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Bibliografski detalji
Izdano u:Int J Mol Sci
Glavni autori: Rodríguez Cruz, Pedro M., Palace, Jacqueline, Beeson, David
Format: Artigo
Jezik:Inglês
Izdano: MDPI 2018
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6032286/
https://ncbi.nlm.nih.gov/pubmed/29874875
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms19061677
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