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A severe collodion phenotype in the newborn period associated with a homozygous missense mutation in ALOX12B

dc.contributor.authorPlagnol, V.
dc.contributor.authorKayserili, H.
dc.contributor.authorKelsell, D. P.
dc.contributor.authorChronnell, C.
dc.contributor.authorBland, P. J.
dc.date.accessioned2021-03-04T17:24:53Z
dc.date.available2021-03-04T17:24:53Z
dc.date.issued2015
dc.identifier.citationBland P. J. , Chronnell C., Plagnol V., Kayserili H., Kelsell D. P. , "A severe collodion phenotype in the newborn period associated with a homozygous missense mutation in ALOX12B", BRITISH JOURNAL OF DERMATOLOGY, cilt.173, sa.1, ss.285-287, 2015
dc.identifier.issn0007-0963
dc.identifier.othervv_1032021
dc.identifier.otherav_85e728e5-b770-412f-96fb-0ff69f7f1151
dc.identifier.urihttp://hdl.handle.net/20.500.12627/91022
dc.identifier.urihttps://doi.org/10.1111/bjd.13627
dc.language.isoeng
dc.subjectKlinik Tıp
dc.subjectDERMATOLOJİ
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectDermatoloji
dc.titleA severe collodion phenotype in the newborn period associated with a homozygous missense mutation in ALOX12B
dc.typeMakale
dc.relation.journalBRITISH JOURNAL OF DERMATOLOGY
dc.contributor.departmentUniversity Of London , ,
dc.identifier.volume173
dc.identifier.issue1
dc.identifier.startpage285
dc.identifier.endpage287
dc.contributor.firstauthorID223233


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