Publication:
Phenotypic heterogeneity in a large Thai slow-channel congenital myasthenic syndrome kinship: Correction

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dc.contributor.authorR. Witoonpanichen_US
dc.contributor.authorT. Pulkesen_US
dc.contributor.authorC. Dejthevapornen_US
dc.contributor.authorP. Witoonpanichen_US
dc.contributor.authorP. Yodnopklaoen_US
dc.contributor.authorS. Wetchaphanphesaten_US
dc.contributor.authorJ. Brengmanen_US
dc.contributor.authorA. G. Engelen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherSurin Hospitalen_US
dc.contributor.otherBurirum Hospitalen_US
dc.contributor.otherMayo Medical Schoolen_US
dc.date.accessioned2018-06-11T05:12:01Z
dc.date.available2018-06-11T05:12:01Z
dc.date.issued2012-05-01en_US
dc.identifier.citationNeuromuscular Disorders. Vol.22, No.5 (2012), 478en_US
dc.identifier.doi10.1016/j.nmd.2012.02.001en_US
dc.identifier.issn18732364en_US
dc.identifier.issn09608966en_US
dc.identifier.other2-s2.0-84859627986en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/14828
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84859627986&origin=inwarden_US
dc.subjectMedicineen_US
dc.subjectNeuroscienceen_US
dc.titlePhenotypic heterogeneity in a large Thai slow-channel congenital myasthenic syndrome kinship: Correctionen_US
dc.typeLetteren_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84859627986&origin=inwarden_US

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