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IFRD1 is a candidate gene for SMNA on chromosome 7q22-q23.
Brkanac Z, Spencer D, Shendure J, Robertson PD, Matsushita M, Vu T, Bird TD, Olson MV, Raskind WH. Brkanac Z, et al. Among authors: matsushita m. Am J Hum Genet. 2009 May;84(5):692-7. doi: 10.1016/j.ajhg.2009.04.008. Epub 2009 Apr 30. Am J Hum Genet. 2009. PMID: 19409521 Free PMC article.
Ataxia-Pancytopenia Syndrome Is Caused by Missense Mutations in SAMD9L.
Chen DH, Below JE, Shimamura A, Keel SB, Matsushita M, Wolff J, Sul Y, Bonkowski E, Castella M, Taniguchi T, Nickerson D, Papayannopoulou T, Bird TD, Raskind WH. Chen DH, et al. Among authors: matsushita m. Am J Hum Genet. 2016 Jun 2;98(6):1146-1158. doi: 10.1016/j.ajhg.2016.04.009. Am J Hum Genet. 2016. PMID: 27259050 Free PMC article.
Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia.
Brkanac Z, Chapman NH, Matsushita MM, Chun L, Nielsen K, Cochrane E, Berninger VW, Wijsman EM, Raskind WH. Brkanac Z, et al. Among authors: matsushita mm. Am J Med Genet B Neuropsychiatr Genet. 2007 Jun 5;144B(4):556-60. doi: 10.1002/ajmg.b.30471. Am J Med Genet B Neuropsychiatr Genet. 2007. PMID: 17450541
2,144 results