A novel splice acceptor site mutation (IVS11 G>A) of PEPD gene causing prolidase deficiency associated with hyperimmunoglobulinemia E
Suri, Deepti, Pandit, Riyaz A., Saini, Arushi Gahlot, Dogra, Sunil, Gupta, Anju, Rawat, Amit, Dwivedi, Isha, Masih, Shet, Attri, Savita VermaVolume:
4
Language:
english
Journal:
Gene Reports
DOI:
10.1016/j.genrep.2016.02.008
Date:
September, 2016
File:
PDF, 944 KB
english, 2016