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Utility of DNA, RNA, Protein, and Functional Approaches to Solve Cryptic Immunodeficiencies.
Cousin, Margot A; Smith, Matthew J; Sigafoos, Ashley N; Jin, Jay J; Murphree, Marine I; Boczek, Nicole J; Blackburn, Patrick R; Oliver, Gavin R; Aleff, Ross A; Clark, Karl J; Wieben, Eric D; Joshi, Avni Y; Pichurin, Pavel N; Abraham, Roshini S; Klee, Eric W.
Afiliación
  • Cousin MA; Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA.
  • Smith MJ; Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
  • Sigafoos AN; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
  • Jin JJ; Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA.
  • Murphree MI; Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, USA.
  • Boczek NJ; Department of Allergy and Immunology, Mayo Clinic, Rochester, MN, USA.
  • Blackburn PR; Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA.
  • Oliver GR; Department of Clinical Genomics, Mayo Clinic, Rochester, MN, USA.
  • Aleff RA; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
  • Clark KJ; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.
  • Wieben ED; Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA.
  • Joshi AY; Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
  • Pichurin PN; Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, USA.
  • Abraham RS; Medical Genome Facility, Mayo Clinic, Rochester, MN, USA.
  • Klee EW; Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA.
J Clin Immunol ; 38(3): 307-319, 2018 04.
Article en En | MEDLINE | ID: mdl-29671115

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Genómica / Proteómica / Síndromes de Inmunodeficiencia Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Infant Idioma: En Revista: J Clin Immunol Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Genómica / Proteómica / Síndromes de Inmunodeficiencia Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Female / Humans / Infant Idioma: En Revista: J Clin Immunol Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos