Heterozygous deletions at the ZEB1 locus verify haploinsufficiency as the mechanism of disease for posterior polymorphous corneal dystrophy type 3.
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| Description | scientific article published on 28 October 2015 |
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author: Alison Hardcastle Petra Lišková Viktor Stránecký Andrea L. Vincent Ľubica Ďuďáková Nicole Carnt Vincent Plagnol |
| Publication date | October 28, 2015 |
| Language | English |
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