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Identification of putative genetic modifying factors that influence the development of Papillon-Lefévre or Haim-Munk syndrome phenotypes.
Pap, É M; Farkas, K; Tóth, L; Fábos, B; Széll, M; Németh, G; Nagy, N.
Affiliation
  • Pap ÉM; Department of Obstetrics and Gynecology Szeged, University of Szeged, Szeged, Hungary.
  • Farkas K; Department of Medical Genetics, University of Szeged, Szeged, Hungary.
  • Tóth L; Department of Medical Genetics, University of Szeged, Szeged, Hungary.
  • Fábos B; Mór Kaposi Teaching Hospital, Kaposvár, Hungary.
  • Széll M; Department of Medical Genetics, University of Szeged, Szeged, Hungary.
  • Németh G; Dermatological Research Group of the Hungarian Academy of Sciences, University of Szeged, Szeged, Hungary.
  • Nagy N; Department of Obstetrics and Gynecology Szeged, University of Szeged, Szeged, Hungary.
Clin Exp Dermatol ; 45(5): 555-559, 2020 Jul.
Article in En | MEDLINE | ID: mdl-31925812
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Papillon-Lefevre Disease / Phenotype / Mutation, Missense / Cathepsin C / Acro-Osteolysis Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Clin Exp Dermatol Year: 2020 Document type: Article Affiliation country: Hungary Country of publication: United kingdom
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Papillon-Lefevre Disease / Phenotype / Mutation, Missense / Cathepsin C / Acro-Osteolysis Type of study: Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Clin Exp Dermatol Year: 2020 Document type: Article Affiliation country: Hungary Country of publication: United kingdom