Novel mutations in the ZEB1 gene identif
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Petra Liskova; Stephen J. Tuft; Rhian Gwilliam; Neil D. Ebenezer; Katerina Jirso
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Article
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2007
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John Wiley and Sons
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English
⚖ 99 KB
We describe the search for mutations in six unrelated Czech and four unrelated British families with posterior polymorphous corneal dystrophy (PPCD); a relatively rare eye disorder. Coding exons and intron/exon boundaries of all three genes (VSX1, COL8A2, and ZEB1/TCF8) previously reported to be imp