Strong evidence that the N21I substitution in the cationic trypsinogen gene causes disease in hereditary pancreatitis

Схожие документы

• Mutations in the cationic trypsinogen gene and evidence for genetic heterogeneity in hereditary pancreatitis
  по: Ferec, C, et al.
  Опубликовано: (1999)
• Misfolding cationic trypsinogen variant p.L104P causes hereditary pancreatitis
  по: Németh, Balázs Csaba, et al.
  Опубликовано: (2016)
• Novel cationic trypsinogen (PRSS1) N29T and R122C mutations cause autosomal dominant hereditary pancreatitis
  по: Pfützer, R, et al.
  Опубликовано: (2002)
• Mutations in exons 2 and 3 of the cationic trypsinogen gene in Japanese families with hereditary pancreatitis
  по: Nishimori, I, et al.
  Опубликовано: (1999)
• Hereditary pancreatitis and mutation of the trypsinogen gene
  по: Weber, P, et al.
  Опубликовано: (1999)