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Novel CARD9 mutation in a patient with chronic invasive dermatophyte infection (tinea profunda).
Nazarian, Rosalynn M; Lilly, Evelyn; Gavino, Christina; Hamilos, Daniel L; Felsenstein, Donna; Vinh, Donald C; Googe, Paul B.
Afiliação
  • Nazarian RM; Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Lilly E; Department of Dermatology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Gavino C; Department of Medicine, McGill University Health Center, and Infectious Disease Susceptibility Program, Research Institute-McGill University Health Centre, Montreal, Quebec, Canada.
  • Hamilos DL; Department of Medicine, Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Felsenstein D; Department of Medicine, Infectious Disease Unit, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Vinh DC; Department of Medicine, McGill University Health Center, and Infectious Disease Susceptibility Program, Research Institute-McGill University Health Centre, Montreal, Quebec, Canada.
  • Googe PB; Department of Dermatology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
J Cutan Pathol ; 47(2): 166-170, 2020 Feb.
Article em En | MEDLINE | ID: mdl-31469433
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tinha do Couro Cabeludo / Candidíase Mucocutânea Crônica / Doenças Genéticas Ligadas ao Cromossomo X / Proteínas Adaptadoras de Sinalização CARD / Mutação com Perda de Função Tipo de estudo: Prognostic_studies Limite: Adult / Humans / Male Idioma: En Revista: J Cutan Pathol Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tinha do Couro Cabeludo / Candidíase Mucocutânea Crônica / Doenças Genéticas Ligadas ao Cromossomo X / Proteínas Adaptadoras de Sinalização CARD / Mutação com Perda de Função Tipo de estudo: Prognostic_studies Limite: Adult / Humans / Male Idioma: En Revista: J Cutan Pathol Ano de publicação: 2020 Tipo de documento: Article