Severe protein C deficiency in a newborn caused by a homozygous pathogenic variant in the PROC gene: a case report
- DOI
- 10.1186/s12887-021-02923-6
- Published
- 2021-10-16
- Container
- BMC Pediatrics
- Publisher
- Springer Science and Business Media LLC
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1186/s12887-021-02923-6,
title = {Severe protein C deficiency in a newborn caused by a homozygous pathogenic variant in the PROC gene: a case report},
author = {Uisook Song and Young Hye Ryu and Kiteak Hong and So-Yeon Shim and Seongyeol Park and Jeong Seok Lee and Young Seok Ju and Seung Han Shin and Soyoung Lee},
year = {2021},
journal = {BMC Pediatrics},
doi = {10.1186/s12887-021-02923-6},
url = {https://doi.org/10.1186/s12887-021-02923-6}
}RIS
TY - JOUR TI - Severe protein C deficiency in a newborn caused by a homozygous pathogenic variant in the PROC gene: a case report AU - Uisook Song AU - Young Hye Ryu AU - Kiteak Hong AU - So-Yeon Shim AU - Seongyeol Park AU - Jeong Seok Lee AU - Young Seok Ju AU - Seung Han Shin AU - Soyoung Lee PY - 2021 JO - BMC Pediatrics DO - 10.1186/s12887-021-02923-6 UR - https://doi.org/10.1186/s12887-021-02923-6 ER -
APA
Song, U., Ryu, Y. H., Hong, K., Shim, S., Park, S., Lee, J. S., Ju, Y. S., Shin, S. H., & Lee, S. (2021). Severe protein C deficiency in a newborn caused by a homozygous pathogenic variant in the PROC gene: a case report. BMC Pediatrics. https://doi.org/10.1186/s12887-021-02923-6
Source records
- crossref · retrieved 2026-11-09T21:11:11.366Z