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

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

DOI Full Paper Access

34

Citations

26

References

2015

Year

Petra Lišková, Cerys J. Evans, Alice E. Davidson, Markéta Žaliová, Ľubica Ďuďáková, Marie Trková, Viktor Stránecký, Nicole Carnt, Vincent Plagnol, Andrea L. Vincent,

European Journal of Human Genetics

Ocular DiseaseMendelian DisorderOphthalmologyGenetic DisorderCorneal DystrophyGeneticsPathologyMolecular GeneticsOcular PathologyHeterozygous DeletionsMedicine

References

	Year	Citations

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