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Use of genome-wide SNP homozygosity mapping in small pedigrees to identify new mutations in VSX2 causing recessive microphthalmia and a semidominant inner retinal dystrophy.
Hum Genet. 2010 Jul;128(1):51-60. doi: 10.1007/s00439-010-0823-6. Epub 2010 Apr 23.
Hum Genet. 2010.
PMID: 20414678
Seeing clearly: the dominant and recessive nature of FOXE3 in eye developmental anomalies.
Iseri SU, Osborne RJ, Farrall M, Wyatt AW, Mirza G, Nürnberg G, Kluck C, Herbert H, Martin A, Hussain MS, Collin JR, Lathrop M, Nürnberg P, Ragoussis J, Ragge NK.
Iseri SU, et al.
Hum Mutat. 2009 Oct;30(10):1378-86. doi: 10.1002/humu.21079.
Hum Mutat. 2009.
PMID: 19708017
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Clinical and genetic features of PKAN patients in a tertiary centre in Turkey.
Akcakaya NH, Iseri SU, Bilir B, Battaloglu E, Tekturk P, Gultekin M, Akar G, Yigiter R, Hanagasi H, Alp R, Cagirici S, Eraksoy M, Ozbek U, Yapici Z.
Akcakaya NH, et al. Among authors: iseri su.
Clin Neurol Neurosurg. 2017 Mar;154:34-42. doi: 10.1016/j.clineuro.2017.01.011. Epub 2017 Jan 15.
Clin Neurol Neurosurg. 2017.
PMID: 28113101
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