TY  - RPRT
TI  - HELLP syndrome associated with factor V R506Q mutation.
AU  - B Brenner
AU  - N Lanir
AU  - I Thaler
PY  - 1996
DO  - 10.1046/j.1365-2141.1996.410947.x
UR  - https://pubmed.ncbi.nlm.nih.gov/8616100/
ID  - 8616100
ER  -