TY  - GEN
AU  - Drévillon,Loïc
AU  - Megarbane,André
AU  - Demeer,Bénédicte
AU  - Matar,Corine
AU  - Benit,Paule
AU  - Briand-Suleau,Audrey
AU  - Bodereau,Virginie
AU  - Ghoumid,Jamal
AU  - Nasser,Mayssa
AU  - Decrouy,Xavier
AU  - Doco-Fenzy,Martine
AU  - Rustin,Pierre
AU  - Gaillard,Dominique
AU  - Goossens,Michel
AU  - Giurgea,Irina
TI  - KBP-cytoskeleton interactions underlie developmental anomalies in Goldberg-Shprintzen syndrome
SN  - 1460-2083
PY  - 2013///1231
KW  - Actins
KW  - genetics
KW  - Adolescent
KW  - Adult
KW  - Child
KW  - Craniofacial Abnormalities
KW  - Female
KW  - France
KW  - Hirschsprung Disease
KW  - Humans
KW  - Infant
KW  - Iraq
KW  - Male
KW  - Microtubules
KW  - Mutation
KW  - Nerve Tissue Proteins
KW  - Pedigree
KW  - Protein Binding
KW  - Tubulin
KW  - White People
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1093/hmg/ddt083
ER  -