학술논문

Hypomorphic mutations of SEC23B gene account for mild phenotypes of congenital dyserythropoietic anemia type II
Document Type
Article
Source
In: Blood Cells, Molecules, and Diseases. (Blood Cells, Molecules, and Diseases, June 2013, 51(1):17-21)
Subject
Language
English
ISSN
10799796
10960961