A novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family

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dc.contributor.authorCallea, M.
dc.contributor.authorNieminen, P.
dc.contributor.authorWilloughby, C. E.
dc.contributor.authorClarich, G.
dc.contributor.authorYavuz, I.
dc.contributor.authorVinciguerra, A.
dc.contributor.authorDi Stazio, M.
dc.date.accessioned2024-04-24T17:11:43Z
dc.date.available2024-04-24T17:11:43Z
dc.date.issued2016
dc.departmentDicle Üniversitesien_US
dc.description.abstract[Abstract Not Available]en_US
dc.identifier.doi10.1111/jdv.12747
dc.identifier.endpage343en_US
dc.identifier.issn0926-9959
dc.identifier.issn1468-3083
dc.identifier.issue2en_US
dc.identifier.pmid25266272
dc.identifier.scopus2-s2.0-84956690676
dc.identifier.scopusqualityQ1
dc.identifier.startpage341en_US
dc.identifier.urihttps://doi.org/10.1111/jdv.12747
dc.identifier.urihttps://hdl.handle.net/11468/17687
dc.identifier.volume30en_US
dc.identifier.wosWOS:000368993100028
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoenen_US
dc.publisherWiley-Blackwellen_US
dc.relation.ispartofJournal of The European Academy of Dermatology and Venereology
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subject[No Keyword]en_US
dc.titleA novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian familyen_US
dc.titleA novel INDEL mutation in the EDA gene resulting in a distinct X- linked hypohidrotic ectodermal dysplasia phenotype in an Italian family
dc.typeLetteren_US

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