A novel splice acceptor site mutation (IVS11 G > A) of PEPD gene causing prolidase deficiency associated with hyperimmunoglobulinemia E

Gene Reports ◽  
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Vol 4 ◽  
pp. 29-32 ◽  
Author(s):  
Deepti Suri ◽  
Riyaz A. Pandit ◽  
Arushi Gahlot Saini ◽  
Sunil Dogra ◽  
Anju Gupta ◽  
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Author(s):  
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Paweł Brzuzan ◽  
Maciej Woźny ◽  
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Dariusz Kaczmarczyk

Gene ◽  
2000 ◽  
Vol 246 (1-2) ◽  
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Rubén A. Dávoli ◽  
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