Examinant per Autoria "Melki, Judith"
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Ítem Accés Obert Loss-of-function mutations in LGI4, a secreted ligand involved in schwann cell myelination, are responsible for arthrogryposis multiplex congenita(Elsevier, 2017) Xue, Shifeng; Gut, Marta; Gut, Ivo Glynne; Melki, Judith
Ítem Accés Obert Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita(BMJ Publishing Group, 2022) Laquerrière, Annie; Gut, Ivo Glynne; Melki, Judith