Fingerprint 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
- Weight
- Alphabetically
Characterization of the molecular defects in RAB27A, caused by RAB27A missense mutations found in patients with Griscelli syndrome
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
45
Citations
(Scopus)