The role of FV 1691G>A, FII 20210G>A mutations and MTHFR 677C>T; 1298A>C and 103G>T FXIII gene polymorphisms in pathogenesis of intraventricular hemorrhage in infants born before 32 weeks of gestation
Crossref DOI link: https://doi.org/10.1007/s00381-017-3460-8
Published Online: 2017-06-03
Published Print: 2017-07
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Szpecht, Dawid
Gadzinowski, Janusz
Seremak-Mrozikiewicz, Agnieszka
Kurzawińska, Grażyna
Drews, Krzysztof
Szymankiewicz, Marta
Funding for this research was provided by:
Poznan University of Medical Sciences (502-14-02215338-09691)
License valid from 2017-06-03