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Enamel Defects in Carriers of a Novel LAMA3 Mutation Underlying Epidermolysis Bullosa

dc.contributor.authorYuen, WY
dc.contributor.authorPasmooij, AM
dc.contributor.authorStellingsma, C
dc.contributor.authorJonkman, MF
dc.date.accessioned2015-05-23T13:59:53Z
dc.date.available2015-05-23T13:59:53Z
dc.date.issued2012-11-01
dc.identifier.issn0001-5555
dc.identifier.issn1651-2057
dc.identifier.urihttp://hdl.handle.net/10026.1/3347
dc.format.extent695-696
dc.format.mediumPrint
dc.languageen
dc.publisherMedical Journals Sweden AB
dc.subjectAdult
dc.subjectAmelogenesis
dc.subjectDNA Mutational Analysis
dc.subjectDental Enamel
dc.subjectDental Enamel Hypoplasia
dc.subjectEpidermolysis Bullosa, Junctional
dc.subjectFemale
dc.subjectGenetic Predisposition to Disease
dc.subjectHaploinsufficiency
dc.subjectHumans
dc.subjectLaminin
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectMutation
dc.subjectPedigree
dc.subjectPhenotype
dc.subjectYoung Adult
dc.titleEnamel Defects in Carriers of a Novel LAMA3 Mutation Underlying Epidermolysis Bullosa
dc.typejournal-article
dc.typeLetter
plymouth.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/22434185
plymouth.issue6
plymouth.volume92
plymouth.publication-statusPublished
plymouth.journalActa Derm Venereol
dc.identifier.doi10.2340/00015555-1341
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Plymouth University Peninsula Schools of Medicine and Dentistry
plymouth.organisational-group/Plymouth/Research Centres
plymouth.organisational-group/Plymouth/Research Centres/Institute of Health and Community
plymouth.organisational-group/Plymouth/Research Centres/Institute of Translational and Stratified Medicine (ITSMED)
plymouth.organisational-group/Plymouth/Research Centres/Institute of Translational and Stratified Medicine (ITSMED)/CBR
plymouth.declined2015-05-23T14:59:53.392+0100
dc.publisher.placeSweden
dc.identifier.eissn1651-2057
rioxxterms.versionofrecord10.2340/00015555-1341


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