Publications by authors named "Lea Durix"

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Expanding the phenotypic and genetic landscape of congenital neutropenia through whole-exome and genome sequencing.
Séverine Marti, Philippe Pellet, Blandine Beaupain, Léa Durix, Julien Buratti

Hemasphere· June 2025

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Association of MPL K39N and R102P heterozygous germline mutations lead to hereditary thrombocytosis.
Emeline Voirin, Anne Bouvier, Isabelle Plo, Léa Durix, Annaëlle Beucher

Am J Hematol· August 2024

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