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Dive into the research topics of 'Characterization of the molecular defects in RAB27A, caused by RAB27A missense mutations found in patients with Griscelli syndrome'. Together they form a unique fingerprint.- Sort by
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Philippe Bahadoran, Roser Busca, Christine Chiaverini, Wendy Westbroek, Jo Lambert, Karine Bille, Gaëlle Valony, Mitsunori Fukuda, Jean Marie Naeyaert, Jean Paul Ortonne, Robert Ballotti
Research output: Contribution to journal › Article › peer-review