reference/5834269

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publicationName	Human Molecular Genetics
startingPage	3577
bibliographicCitation	Chevessier F, Girard E, Molgó J, Bartling S, Koenig J, Hantaï D, Witzemann V. A mouse model for congenital myasthenic syndrome due to MuSK mutations reveals defects in structure and function of neuromuscular junctions. Hum Mol Genet. 2008 Nov 15;17(22):3577–95. doi: 10.1093/hmg/ddn251. PMID: 18718936.
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date	2008-08-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1093/hmg/ddn251 https://pubmed.ncbi.nlm.nih.gov/18718936
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	A mouse model for congenital myasthenic syndrome due to MuSK mutations reveals defects in structure and function of neuromuscular junctions
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