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

dc.contributor.author	Ratnasamy, Vithiya
dc.contributor.author	Suganthan, N.
dc.contributor.author	Sirisena, Nirmala Dushyanthi
dc.contributor.author	Grüning, Nana-Maria
dc.contributor.author	Brandau, Oliver
dc.contributor.author	Kumanan, T.
dc.contributor.author	Dagnall, Casey L.
dc.contributor.author	McReynolds, Lisa J.
dc.contributor.author	Savage, Sharon A.
dc.contributor.author	Dissanayake, Vajira H. W.
dc.date.accessioned	2022-09-26T05:40:48Z
dc.date.available	2022-09-26T05:40:48Z
dc.date.issued	2018
dc.identifier.citation	BMC Medical Genetics (2018) 19:85	en_US
dc.identifier.uri	http://repo.lib.jfn.ac.lk/ujrr/handle/123456789/7518
dc.language.iso	en	en_US
dc.subject	DKC1	en_US
dc.subject	Dyskeratosis congenita	en_US
dc.subject	Nail dystrophy	en_US
dc.subject	Oral leukoplakia	en_US
dc.subject	Pancytopenia	en_US
dc.subject	Skin pigmentation	en_US
dc.title	Dyskeratosis congenita with a novel genetic variant in the DKC1 gene: a case report	en_US
dc.type	Case report	en_US