Associated Papers
A case of Feingold type 2 syndrome associated with keratoconus refines keratoconus type 7 locus on chromosome 13q.
Sirchia F et al.
European Journal of Medical Genetics, 2017
Molecular Screening of Keratoconus Susceptibility Sequence Variants in VSX1, TGFBI, DOCK9, STK24, and IPO5 Genes in Polish Patients and Novel TGFBI Variant Identification.
Karolak JA et al.
Ophthalmic Genetics, 2016
Novel mutation and three other sequence variants segregating with phenotype at keratoconus 13q32 susceptibility locus.
Czugala M et al.
European Journal of Human Genetics : Ejhg, 2012
Sequence variants in COL4A1 and COL4A2 genes in Ecuadorian families with keratoconus.
Karolak JA et al.
Molecular Vision, 2011
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