Dyskeratosis congenita with a novel genetic variant in the DKC1 gene: a case report

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dc.contributor.authorRatnasamy, Vithiya
dc.contributor.authorSuganthan, N.
dc.contributor.authorSirisena, Nirmala Dushyanthi
dc.contributor.authorGrüning, Nana-Maria
dc.contributor.authorBrandau, Oliver
dc.contributor.authorKumanan, T.
dc.contributor.authorDagnall, Casey L.
dc.contributor.authorMcReynolds, Lisa J.
dc.contributor.authorSavage, Sharon A.
dc.contributor.authorDissanayake, Vajira H.W.
dc.date.accessioned2022-09-26T05:40:48Z
dc.date.available2022-09-26T05:40:48Z
dc.date.issued2018
dc.identifier.citationBMC Medical Genetics (2018) 19:85en_US
dc.identifier.urihttp://repo.lib.jfn.ac.lk/ujrr/handle/123456789/7518
dc.language.isoenen_US
dc.subjectDKC1en_US
dc.subjectDyskeratosis congenitaen_US
dc.subjectNail dystrophyen_US
dc.subjectOral leukoplakiaen_US
dc.subjectPancytopeniaen_US
dc.subjectSkin pigmentationen_US
dc.titleDyskeratosis congenita with a novel genetic variant in the DKC1 gene: a case reporten_US
dc.typeCase reporten_US

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