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Year | Number of Results |
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2015 | 1 |
2016 | 2 |
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Altered expression of Crb2 in podocytes expands a variation of CRB2 mutations in steroid-resistant nephrotic syndrome.
Pediatr Nephrol. 2017 May;32(5):801-809. doi: 10.1007/s00467-016-3549-4. Epub 2016 Dec 10.
Pediatr Nephrol. 2017.
PMID: 27942854
A case report of CRB2 mutation identified in a Chinese boy with focal segmental glomerulosclerosis.
Fan J, Fu R, Ren F, He J, Wang S, Gou M.
Fan J, et al.
Medicine (Baltimore). 2018 Sep;97(37):e12362. doi: 10.1097/MD.0000000000012362.
Medicine (Baltimore). 2018.
PMID: 30212996
Free PMC article.
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Defects of CRB2 cause steroid-resistant nephrotic syndrome.
Ebarasi L, Ashraf S, Bierzynska A, Gee HY, McCarthy HJ, Lovric S, Sadowski CE, Pabst W, Vega-Warner V, Fang H, Koziell A, Simpson MA, Dursun I, Serdaroglu E, Levy S, Saleem MA, Hildebrandt F, Majumdar A.
Ebarasi L, et al.
Am J Hum Genet. 2015 Jan 8;96(1):153-61. doi: 10.1016/j.ajhg.2014.11.014. Epub 2014 Dec 31.
Am J Hum Genet. 2015.
PMID: 25557779
Free PMC article.
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Expansion of phenotype and genotypic data in CRB2-related syndrome.
Lamont RE, Tan WH, Innes AM, Parboosingh JS, Schneidman-Duhovny D, Rajkovic A, Pappas J, Altschwager P, DeWard S, Fulton A, Gray KJ, Krall M, Mehta L, Rodan LH, Saller DN Jr, Steele D, Stein D, Yatsenko SA, Bernier FP, Slavotinek AM.
Lamont RE, et al.
Eur J Hum Genet. 2016 Oct;24(10):1436-44. doi: 10.1038/ejhg.2016.24. Epub 2016 Mar 23.
Eur J Hum Genet. 2016.
PMID: 27004616
Free PMC article.
Review.
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