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GGCX mutations show different responses to vitamin K thereby determining the severity of the hemorrhagic phenotype in VKCFD1 patients.
Ghosh S, Kraus K, Biswas A, Müller J, Buhl AL, Forin F, Singer H, Höning K, Hornung V, Watzka M, Czogalla-Nitsche KJ, Oldenburg J. Ghosh S, et al. Among authors: czogalla nitsche kj. J Thromb Haemost. 2021 Jun;19(6):1412-1424. doi: 10.1111/jth.15238. Epub 2021 May 4. J Thromb Haemost. 2021. PMID: 33590680 Free article.