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Springer Nature [academic journals on nature.com], European Journal of Human Genetics, 7(24), p. 985-991, 2015

DOI: 10.1038/ejhg.2015.232

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

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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