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Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1

✍ Scribed by Finlayson, S.; Palace, J.; Belaya, K.; Walls, T. J.; Norwood, F.; Burke, G.; Holton, J. L.; Pascual-Pascual, S. I.; Cossins, J.; Beeson, D.

Book ID: 121342613
Publisher: BMJ Publishing Group
Year: 2013
Tongue: English
Weight: 374 KB
Volume: 84
Category: Article
ISSN: 0022-3050
DOI: 10.1136/jnnp-2012-304716

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