Autoantibodies to N-terminally truncated GAD improve clinical phenotyping of individuals with adult-onset diabetes: Action LADA 12

Research output: Contribution to journal › Research article › Contributed › peer-review

Contributors

  • Peter Achenbach - (Author)
  • Mohammed I. Hawa - (Author)
  • Stephanie Krause - (Author)
  • Vito Lampasona - (Author)
  • Samuel T. Jerram - (Author)
  • Alistair J. K. Williams - (Author)
  • Ezio Bonifacio - , Chair of Preclinical stem cell therapy and diabetes (Author)
  • Anette G. Ziegler - (Author)
  • R. David Leslie - (Author)

Details

Original languageEnglish
Pages (from-to)1644-1649
JournalDiabetologia
Volume61
Issue number7
Publication statusPublished - Jul 2018
Peer-reviewedYes

External IDs

Scopus 85044927952
ORCID /0000-0002-8704-4713/work/141544297

Keywords

Research priority areas of TU Dresden

DFG Classification of Subject Areas according to Review Boards

Sustainable Development Goals

Keywords

  • Adult-onset diabetes, Autoantibodies, Autoimmune, Clinical phenotype, GAD, LADA, N-terminally truncated GAD65, Patients, Type 1 diabetes

Library keywords