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PubMed (OMIM) for id: 333142

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Mutations of the catalytic subunit of RAB3GAP cause Warburg Micro syndrome.
Aligianis IA, Johnson CA, Gissen P, Chen D, Hampshire D, Hoffmann K, Maina EN, Morgan NV, Tee L, Morton J, Ainsworth JR, Horn D, Rosser E, Cole TR, Stolte-Dijkstra I, Fieggen K, Clayton-Smith J, Mégarbané A, Shield JP, Newbury-Ecob R, Dobyns WB, Graham JM Jr, Kjaer KW, Warburg M, Bond J, Trembath RC, Harris LW, Takai Y, Mundlos S, Tannahill D, Woods CG, Maher ER. Aligianis IA, et al. Nat Genet. 2005 Mar;37(3):221-3. doi: 10.1038/ng1517. Nat Genet. 2005. PMID: 15696165
Micro syndrome in Muslim Pakistan children.
Ainsworth JR, Morton JE, Good P, Woods CG, George ND, Shield JP, Bradbury J, Henderson MJ, Chhina J. Ainsworth JR, et al. Ophthalmology. 2001 Mar;108(3):491-7. doi: 10.1016/s0161-6420(00)00540-6. Ophthalmology. 2001. PMID: 11237903
A second family with Micro syndrome.
Rodríguez Criado G, Rufo M, Gómez de Terreros I. Rodríguez Criado G, et al. Clin Dysmorphol. 1999 Oct;8(4):241-5. Clin Dysmorphol. 1999. PMID: 10532171