A novel splice acceptor site mutation (IVS11 G > A) of PEPD gene causing prolidase deficiency associated with hyperimmunoglobulinemia E
2003 ◽
Vol 40
(8)
◽
pp. 102e-102
◽
Keyword(s):
2010 ◽
Vol 302
(9)
◽
pp. 701-703
◽
2000 ◽
Vol 15
(1)
◽
pp. 120-120
◽
2018 ◽
Vol 179
(2)
◽
pp. 206-218
◽
Keyword(s):
1990 ◽
Vol 265
(32)
◽
pp. 19716-19720
◽
Keyword(s):