The Role of GRP and MGP in the Development of Non-Hemorrhagic VKCFD1 Phenotypes

Vitamin K dependent coagulation factor deficiency type 1 (VKCFD1) is a rare hereditary bleeding disorder caused by mutations in γ-Glutamyl carboxylase (GGCX) gene. The GGCX enzyme catalyzes the γ-carboxylation of 15 different vitamin K dependent (VKD) proteins, which have function in blood coagulati...

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Detalles Bibliográficos
Autores principales: Ghosh, Suvoshree, Oldenburg, Johannes, Czogalla-Nitsche, Katrin J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8775833/
https://www.ncbi.nlm.nih.gov/pubmed/35054981
http://dx.doi.org/10.3390/ijms23020798

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8775833/
https://www.ncbi.nlm.nih.gov/pubmed/35054981
http://dx.doi.org/10.3390/ijms23020798

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