Lack of NPHP2 mutations in a newborn infant with Joubert syndrome-related disorder presenting as end-stage renal disease

2007 ◽  
Vol 22 (5) ◽  
pp. 750-752 ◽  
Author(s):  
Farahnak Assadi
Author(s):  
Aysun Karabay Bayazit ◽  
Bahriye Atmiş ◽  
Engin Melek ◽  
Abdulsamet Ala ◽  
Merve Sapmaz ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document