A Case of Allgrove Syndrome with a Novel IVS7 +1 G>A Mutation of The AAAS Gene

مواد مشابهة

• Mutations of the AAAS gene in an Indian family with Allgrove's syndrome
  بواسطة: Mukhopadhya, Ashis, وآخرون
  منشور في: (2006)
• Alacrima as a Harbinger of Adrenal Insufficiency in a Child with Allgrove (AAA) Syndrome
  بواسطة: Brown, Brande, وآخرون
  منشور في: (2016)
• Identification of AAAS gene mutation in Allgrove syndrome: A report of three cases
  بواسطة: LI, WENJING, وآخرون
  منشور في: (2015)
• A novel NR3C2 mutation in a Japanese patient with the renal form of pseudohypoaldosteronism type 1
  بواسطة: Tsunogai, Toshiki, وآخرون
  منشور في: (2016)
• Clinical and molecular report of c.1331 + 1G > A mutation of the AAAS gene in a Moroccan family with Allgrove syndrome: a case report
  بواسطة: Berrani, H., وآخرون
  منشور في: (2018)