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Novel variants of CYP21A2 in Vietnamese patients with congenital adrenal hyperplasia.

Dung V ChiThinh H TranDuc H NguyenLong H LuongPhuong T LeMinh H TaHuong T T NgoMai P NguyenTuan P Le-AnhDat P NguyenThe-Hung BuiVan T TaVan-Khanh Tran
Published in: Molecular genetics & genomic medicine (2019)
The result will contribute in further understanding the genotype-phenotype relationship of CAH patients and to guide better treatment and management of the affected.
Keyphrases
  • end stage renal disease
  • ejection fraction
  • chronic kidney disease
  • peritoneal dialysis
  • gene expression
  • patient reported outcomes
  • combination therapy