Reassessment of the putative role of BLK-p.A71T loss-of-function mutation in MODY and type 2 diabetes

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • A Bonnefond
  • L Yengo
  • J Philippe
  • A Dechaume
  • I Ezzidi
  • E Vaillant
  • A P Gjesing
  • E A Andersson
  • S Czernichow
  • S Hercberg
  • S Hadjadj
  • G Charpentier
  • O Lantieri
  • B Balkau
  • M Marre
  • Pedersen, Oluf Borbye
  • Hansen, Torben
  • P Froguel
  • M Vaxillaire
MODY is believed to be caused by at least 13 different genes. Five rare mutations at the BLK locus, including only one non-synonymous p.A71T variant, were reported to segregate with diabetes in three MODY families. The p.A71T mutation was shown to abolish the enhancing effect of BLK on insulin content and secretion from pancreatic beta cell lines. Here, we reassessed the contribution of BLK to MODY and tested the effect of BLK-p.A71T on type 2 diabetes risk and variations in related traits.
OriginalsprogEngelsk
TidsskriftDiabetologia
Vol/bind56
Udgave nummer3
Sider (fra-til)492-496
Antal sider5
ISSN0012-186X
DOI
StatusUdgivet - mar. 2013

ID: 45583318