TY  - GEN
AU  - Paraboschi,E M
AU  - Kayiran,S M
AU  - Özbek,N
AU  - Gürakan,B
AU  - Peyvandi,F
AU  - Guella,I
AU  - Duga,S
AU  - Asselta,R
TI  - Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency
SN  - 1365-2516
PY  - 2012///0502
KW  - Factor V
KW  - genetics
KW  - Factor V Deficiency
KW  - Frameshift Mutation
KW  - Humans
KW  - Infant
KW  - Male
KW  - Mutation, Missense
KW  - Sequence Analysis, DNA
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1111/j.1365-2516.2011.02621.x
ER  -