| 1 | GAMOS1, WDR73
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| Extending the ophthalmological phenotype of Galloway-Mowat syndrome with distinct retinal dysfunction: a report and review of ocular findings.
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| Al-Rakan MA, Abothnain MD, Alrifai MT, Alfadhel M.
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| BMC Ophthalmol 18(1):147. doi: 10.1186/s12886-018-0820-4. Review.
2018
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| 2 | GAMOS1, WDR73
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| Loss-of-Function Mutations in WDR73 Are Responsible for Microcephaly and Steroid-Resistant Nephrotic Syndrome: Galloway-Mowat Syndrome.
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| Colin E, Huynh Cong E, Mollet G, Guichet A, Gribouval O, Arrondel C, Boyer O, Daniel L, Gubler MC, Ekinci Z, Tsimaratos M, Chabrol B, Boddaert N, Verloes A, Chevrollier A, Gueguen N, Desquiret-Dumas V, Ferré M, Procaccio V, Richard L, Funalot B, Moncla A, Bonneau D, Antignac C.
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| Am J Hum Genet 95(6):637-48. doi: 10.1016/j.ajhg.2014.10.011. Epub 2014 Nov 13. 2014
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| 3 | GAMOS1
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| Galloway-Mowat syndrome: neurologic features in two sibling pairs.
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| Ekstrand JJ, Friedman AL, Stafstrom CE.
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| Pediatr Neurol 47(2):129-32. doi: 10.1016/j.pediatrneurol.2012.04.011. 2012
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| 4 | GAMOS1
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| Collapsing glomerulopathy in Galloway-Mowat syndrome: a case report and review of the literature.
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| Sartelet H, Pietrement C, Noel LH, Sabouraud P, Birembaut P, Oligny LL, Roussel B, Doco-Fenzy M.
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| Pathol Res Pract 204(6):401-6. doi: 10.1016/j.prp.2007.12.007. Epub 2008 Feb 13. 2008
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| 5 | GAMOS1, GAMOS2, GAMOS3, GAMOS4, GAMOS5, GAMOS6, GAMOS7, GAMOS8
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| Galloway-Mowat syndrome: a glomerular basement membrane disorder?
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| Lin CC, Tsai JD, Lin SP, Tzen CY, Shen EY, Shih CS.
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| Pediatr Nephrol 16(8):653-7. 2001
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| 6 | GAMOS1
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| Congenital microcephaly, infantile spasms, psychomotor retardation, and nephrotic syndrome in two sibs.
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| Roos RA, Maaswinkel-Mooy PD, vd Loo EM, Kanhai HH.
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| Eur J Pediatr 146(5):532-6. 1987
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