It is a congenital generalized malabsorptive disease associated with a lack of EE cells in the small intestine and colon secondary to mutations in NEUROG 3
暂无分享,去创建一个
Martín G. Martín | D. Gui | G. Cortina | Steven J. Ohsie | D. Kahana | Garrett Gerney BAa | Martín G. Martín