TY  - GEN
AU  - Aminkeng,F
TI  - PDGFRB mutation causes autosomal-dominant Penttinen syndrome
SN  - 1399-0004
PY  - 2016///0208
KW  - Acro-Osteolysis
KW  - genetics
KW  - Female
KW  - Humans
KW  - Limb Deformities, Congenital
KW  - Male
KW  - Point Mutation
KW  - Progeria
KW  - Receptor, Platelet-Derived Growth Factor beta
KW  - Signal Transduction
N1  - Publication Type: Journal Article; Comment
UR  - https://doi.org/10.1111/cge.12680
ER  -