scholarly journals Two Novel AGXT Mutations Cause the Infantile Form of Primary Hyperoxaluria Type I in a Chinese Family: Research on Missed Mutation

2019 ◽  
Vol 10 ◽  
Author(s):  
Xiulan Lu ◽  
Weijian Chen ◽  
Liping Li ◽  
Xinyuan Zhu ◽  
Caizhi Huang ◽  
...  
2018 ◽  
Vol 34 (2) ◽  
pp. 319-327 ◽  
Author(s):  
Alexandra Bruel ◽  
Justine Bacchetta ◽  
Tiphanie Ginhoux ◽  
Christelle Rodier-Bonifas ◽  
Anne-Laure Sellier-Leclerc ◽  
...  

Nephron ◽  
1993 ◽  
Vol 63 (2) ◽  
pp. 217-221 ◽  
Author(s):  
P. Calzavara ◽  
M. Marangelld ◽  
M. Petrarulo ◽  
P. Ballanti ◽  
E. Bonucci ◽  
...  

1991 ◽  
Vol 90 (2) ◽  
pp. 179-188 ◽  
Author(s):  
Richard W.E. Watts ◽  
Stephen H. Morgan ◽  
Christopher J. Danpure ◽  
Paul Purkiss ◽  
Roy Y. Calne ◽  
...  

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