Heterozygous deletions at the ZEB1 locus verify...

European Journal of Human Genetics 2015 / 10

Heterozygous deletions at the ZEB1 locus verify haploinsufficiency as the mechanism of disease for posterior polymorphous corneal dystrophy type 3

Liskova, Petra, Evans, Cerys J, Davidson, Alice E, Zaliova, Marketa, Dudakova, Lubica, Trkova, Marie, Stranecky, Viktor, Carnt, Nicole, Plagnol, Vincent, Vincent, Andrea L, Tuft, Stephen J, Hardcastle
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Language:
english
Journal:
European Journal of Human Genetics
DOI:
10.1038/ejhg.2015.232
Date:
October, 2015
File:
PDF, 1.00 MB
english, 2015
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