KBP-cytoskeleton interactions underlie developmental anomalies in Goldberg-Shprintzen syndrome.
Drévillon L; Megarbane A; Demeer B; Matar C; Benit P; Briand-Suleau A; Bodereau V; Ghoumid J; Nasser M; Decrouy X; Doco-Fenzy M; Rustin P; Gaillard D; Goossens M; Giurgea I; Human Molecular Genetics, 2013, vol. 22, issue 12, p 2387, ISSN 14602083. ISBN 14602083.

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