Article Versions Notes

Shinozuka J, Okumura N, Nagasawa M, Nishikado M, Kadowaki S, Katsuda I, Imashuku S. Congenital Hypofibrinogenemia in a Neonate with a Novel Mutation in the FGB Gene. Pediatric Reports. 2021; 13(1):113-117. https://doi.org/10.3390/pediatric13010016

Shinozuka, Jun, Nobuo Okumura, Mayumi Nagasawa, Motokazu Nishikado, Sayaka Kadowaki, Itsuro Katsuda, and Shinsaku Imashuku. 2021. "Congenital Hypofibrinogenemia in a Neonate with a Novel Mutation in the FGB Gene" Pediatric Reports 13, no. 1: 113-117. https://doi.org/10.3390/pediatric13010016

Shinozuka, J., Okumura, N., Nagasawa, M., Nishikado, M., Kadowaki, S., Katsuda, I., & Imashuku, S. (2021). Congenital Hypofibrinogenemia in a Neonate with a Novel Mutation in the FGB Gene. Pediatric Reports, 13(1), 113-117. https://doi.org/10.3390/pediatric13010016