Familial vitamin K metabolism deficiency responsible for a congenital binder phenotype. Grammatopoulos K, Harroche A, Peduto C, Vegas N, et al. Arch Pediatr 2025 Jun 25:S0929-693X(25)00101.

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Grammatopoulos K, Harroche A, Peduto C, Vegas N, et al. Familial vitamin K metabolism deficiency responsible for a congenital binder phenotype. Arch Pediatr 2025 Jun 25:S0929-693X(25)00101.
PMID: 40562611