Article ID Journal Published Year Pages File Type
5589024 European Journal of Medical Genetics 2017 4 Pages PDF
Abstract
In conclusion, we report a novel phenotypic association of Feingold syndrome type 2 and keratoconus, a likely contiguous gene syndrome due to a large genomic deletion on 13q spanning MIR17HG and a still to be identified gene for keratoconus.
Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Genetics
Authors
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