A neonate with homozygous protein C deficiency with a homozygous Arg178Trp mutation.
Ozlu F, Kyotani M, Taskin E, Ozcan K, Kojima T, Matsushita T, Yapicioğlu H, Takagi A, Saşmaz I, Satar M, Narli N.
Ozlu F, et al. Among authors: taskin e.
J Pediatr Hematol Oncol. 2008 Aug;30(8):608-11. doi: 10.1097/MPH.0b013e318179a15d.
J Pediatr Hematol Oncol. 2008.
PMID: 18799939