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Novel mutations in the WFS1 gene are associated with Wolfram syndrome and systemic inflammation.
Panfili, Eleonora; Mondanelli, Giada; Orabona, Ciriana; Belladonna, Maria L; Gargaro, Marco; Fallarino, Francesca; Orecchini, Elena; Prontera, Paolo; Proietti, Elisa; Frontino, Giulio; Tirelli, Eva; Iacono, Alberta; Vacca, Carmine; Puccetti, Paolo; Grohmann, Ursula; Esposito, Susanna; Pallotta, Maria T.
Affiliation
  • Panfili E; Department of Medicine and Surgery, University of Perugia, Perugia, 06132, Italy.
  • Mondanelli G; Department of Medicine and Surgery, University of Perugia, Perugia, 06132, Italy.
  • Orabona C; Department of Medicine and Surgery, University of Perugia, Perugia, 06132, Italy.
  • Belladonna ML; Department of Medicine and Surgery, University of Perugia, Perugia, 06132, Italy.
  • Gargaro M; Department of Medicine and Surgery, University of Perugia, Perugia, 06132, Italy.
  • Fallarino F; Department of Medicine and Surgery, University of Perugia, Perugia, 06132, Italy.
  • Orecchini E; Department of Medicine and Surgery, University of Perugia, Perugia, 06132, Italy.
  • Prontera P; Medical Genetics Unit, University-Hospital "Santa Maria della Misericordia", Perugia, 06132, Italy.
  • Proietti E; Department of Medicine and Surgery, University of Perugia, Perugia, 06132, Italy.
  • Frontino G; Department of Pediatrics, Diabetes Research Institute, IRCCS San Raffaele Hospital, Milan, 20132, Italy.
  • Tirelli E; Department of Pediatrics, Diabetes Research Institute, IRCCS San Raffaele Hospital, Milan, 20132, Italy.
  • Iacono A; Department of Medicine and Surgery, University of Perugia, Perugia, 06132, Italy.
  • Vacca C; Department of Medicine and Surgery, University of Perugia, Perugia, 06132, Italy.
  • Puccetti P; Department of Medicine and Surgery, University of Perugia, Perugia, 06132, Italy.
  • Grohmann U; Department of Medicine and Surgery, University of Perugia, Perugia, 06132, Italy.
  • Esposito S; Visiting Professor, Department of Pathology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
  • Pallotta MT; Pediatric Clinic Pietro Barilla Children's Hospital, Department of Medicine and Surgery, Università di Parma, Parma, 43126, Italy.
Hum Mol Genet ; 30(3-4): 265-276, 2021 04 26.
Article in En | MEDLINE | ID: mdl-33693650
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Wolfram Syndrome / Leukocytes, Mononuclear / Inflammation / Membrane Proteins / Mutation Type of study: Prognostic_studies / Risk_factors_studies Limits: Child / Female / Humans Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2021 Document type: Article Affiliation country:
Fulltext
Add to My VHL
Print
XML
PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Wolfram Syndrome / Leukocytes, Mononuclear / Inflammation / Membrane Proteins / Mutation Type of study: Prognostic_studies / Risk_factors_studies Limits: Child / Female / Humans Language: En Journal: Hum Mol Genet Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2021 Document type: Article Affiliation country: