Molecular basis of transient neonatal diabetes mellitus in Japan: frequent KATP-TNDM and identification of a patient with a monoallelic INS mutation

類似資料

• Focal form of congenital hyperinsulinism clearly detectable by contrast-enhanced computed tomography imaging
  著者:: Hashimoto, Yukiko, 等
  出版事項: (2015)
• Chromosome 6q24-related diabetes mellitus
  著者:: Yorifuji, Tohru, 等
  出版事項: (2018)
• Acute Myeloid Leukemia With RBM15-MKL1 Presenting as Severe Hepatic Failure
  著者:: Nakano, Yoshiko, 等
  出版事項: (2017)
• Nationwide survey of endogenous hyperinsulinemic hypoglycemia in Japan (2017–2018): Congenital hyperinsulinism, insulinoma, non‐insulinoma pancreatogenous hypoglycemia syndrome and insulin autoimmune syndrome (Hirata’s disease)
  著者:: Yamada, Yuki, 等
  出版事項: (2019)
• Frequent monoallelic or skewed expression for developmental genes in CNS-derived cells and evidence for balancing selection
  著者:: Branciamore, Sergio, 等
  出版事項: (2018)