A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1

Lignende værker

• The Levels of Serum Low-Density Lipoprotein Cholesterol Using Direct Measurement in Healthy Japanese School Children
  af: Ogawa, Yohei, et al.
  Udgivet: (2004)
• The Relationship between Preheparin Lipoprotein Lipase and Metabolic Derangements in Obese Japanese Children
  af: Abe, Yuki, et al.
  Udgivet: (2011)
• Autosomal dominant muscle cramp syndrome in a Japanese family
  af: Chiba, S, et al.
  Udgivet: (1999)
• H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency
  af: Nagasaki, Keisuke, et al.
  Udgivet: (2009)
• A study of the etiology of transient congenital hypothyroidism in Niigata Prefecture, Japan
  af: Nagasaki, Keisuke, et al.
  Udgivet: (2013)