Novel Gamma-Glutamyl Carboxylase Mutation Causing Hemorrhagic and Non-Hemorrhagic VKCFD1 Phenotypes von Guzzardo, Gianna M., Ghosh, Suvoshree, Pezeshkpoor, Behnaz, Pavlova, Anna, Czogalla-Nitsche, Katrin, Oldenburg, Johannes, Chitlur, Meera B.

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The Role of GRP and MGP in the Development of Non-Hemorrhagic VKCFD1 Phenotypes von Ghosh, Suvoshree, Oldenburg, Johannes, Czogalla-Nitsche, Katrin J

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GGCX mutations show different responses to vitamin K thereby determining the severity of the hemorrhagic phenotype in VKCFD1 patients von Ghosh, Suvoshree, Kraus, Katrin, Biswas, Arijit, Müller, Jens, Buhl, Anna‐Lena, Forin, Francesco, Singer, Heike, Höning, Klara, Hornung, Veit, Watzka, Matthias, Czogalla‐Nitsche, Katrin J., Oldenburg, Johannes

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GGCX variants leading to biallelic deficiency to γ‐carboxylate GRP cause skin laxity in VKCFD1 patients von Ghosh, Suvoshree, Kraus, Katrin, Biswas, Arijit, Müller, Jens, Forin, Francesco, Singer, Heike, Höning, Klara, Hornung, Veit, Watzka, Matthias, Oldenburg, Johannes, Czogalla‐Nitsche, Katrin J.

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Variants in FIX propeptide associated with vitamin K antagonist hypersensitivity: functional analysis and additional data confirming the common founder mutations von Pezeshkpoor, Behnaz, Czogalla, Katrin J., Caspers, Michael, Berkemeier, Ann-Cristin, Liphardt, Kerstin, Ghosh, Suvoshree, Kellner, Marco, Ulrich, Silvia, Pavlova, Anna, Oldenburg, Johannes

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