SPINK5 mutation and FLGgene deletion in an infant with nethertonsyndrome

Yakut, TahsinKarkucak, MutluÖvünç Hacıhamdioğlu, DuyguFerhatoğlu, Zeynep AltanFişek İzci, Neslihan Müge2022-05-232022-05-232022Hacıhamdioğlu DÖ, Altan Ferhatoğlu Z, Karkucak M, Fişek İzci NM, Yakut T. SPINK5 mutation and FLG gene deletion in an infant with Netherton syndrome. Pediatr Int. 2022 Jan;64(1):e15087. doi: 10.1111/ped.15087. PMID: 35438212.1442-200Xhttp://doi.org/10.1111/ped.15087https://hdl.handle.net/20.500.12713/2703No Abstract Aviableeninfo:eu-repo/semantics/closedAccessSPINK5FilaggrinNetherton SyndromeSPINK5 mutation and FLGgene deletion in an infant with nethertonsyndromeArticle64135438212WOS:0007835085000012-s2.0-85128514394Q410.1111/ped.15087Q3