A new human nherf1 mutation decreases renal phosphate transporter npt2a expression by a pth- independent mechanism

HIGHLIGHTS

• who: Bernard Grandchamp and colleagues from the Diderot, Paris, France, Department of Pharmacology, School of Medicine, Emory University, Atlanta, Georgia, United States of America, Service de Physiologie Explorations Fonctionnelles, Hôpital Européen Georges Pompidou, Paris, France have published the article: A New Human NHERF1 Mutation Decreases Renal Phosphate Transporter NPT2a Expression by a PTH- Independent Mechanism, in the Journal: (JOURNAL) of April/10,/2012
• what: The authors identified in a patient with inappropriate renal phosphate reabsorption a previously unidentified mutation (E68A) located in the PDZ1 domain of NHERF1. the authors report the consequences of . . .
  

   

  

  If you want to have access to all the content you need to log in!

  Thanks :)

  Username or Email

  Password

  Remember me

  Lost your password?

  If you don't have an account, you can create one here.