TY  - RPRT
TI  - A novel fibrinogen gamma-chain mutation, p. γAla327Val, causes structural abnormality of D region and ultimately leads to congenital dysfibrinogenemia
AU  - Wei, A.
AU  - Wu, Y.
AU  - Xiang, L.
AU  - Yan, J.
AU  - Cheng, P.
AU  - Deng, D.
AU  - Lin, F.
PY  - 2020
DO  - 10.1101/2020.01.29.925172
UR  - https://www.biorxiv.org/content/10.1101/2020.01.29.925172v1
ID  - 10.1101/2020.01.29.925172
ER  -