Diazoxide-unresponsive congenital hyperinsulinism associated with ABCC8 nonsense mutation

Benzer Materyaller

• A novel mutation of ABCC8 gene in a patient with diazoxide-unresponsive congenital hyperinsulinism
  Yazar:: Park, Ji Sook, ve diğerleri
  Baskı/Yayın Bilgisi: (2016)
• Partial diazoxide responsiveness in a neonate with hyperinsulinism due to homozygous ABCC8 mutation
  Yazar:: Kiff, Sarah, ve diğerleri
  Baskı/Yayın Bilgisi: (2019)
• Monoallelic ABCC8 mutations are a common cause of diazoxide-unresponsive diffuse form of congenital hyperinsulinism
  Yazar:: Saint-Martin, Cécile, ve diğerleri
  Baskı/Yayın Bilgisi: (2014)
• Birth weight and diazoxide unresponsiveness strongly predict the likelihood of congenital hyperinsulinism due to a mutation in ABCC8 or KCNJ11
  Yazar:: Hewat, Thomas I., ve diğerleri
  Baskı/Yayın Bilgisi: (2021)
• Paternally inherited ABCC8 mutation causing diffuse congenital hyperinsulinism
  Yazar:: Chandran, Suresh, ve diğerleri
  Baskı/Yayın Bilgisi: (2013)