| Literature DB >> 23458718 |
Inga Koneczny1, Judith Cossins, Angela Vincent.
Abstract
MuSK myasthenia gravis is a rare, severe autoimmune disease of the neuromuscular junction, only identified in 2001, with unclear pathogenic mechanisms. In this review we describe the clinical aspects that distinguish MuSK MG from AChR MG, review what is known about the role of MuSK in the development and function of the neuromuscular junction, and discuss the data that address how the antibodies to MuSK lead to neuromuscular transmission failure.Entities:
Keywords: AChR; DOK7; IgG4; LRP4; MG; RAPSN; muscle-specific tyrosine kinase; myasthenia gravis; neuromuscular transmission; quantal content
Mesh:
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Year: 2013 PMID: 23458718 PMCID: PMC3867884 DOI: 10.1111/joa.12034
Source DB: PubMed Journal: J Anat ISSN: 0021-8782 Impact factor: 2.610