| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5589024 | European Journal of Medical Genetics | 2017 | 4 Pages |
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.
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Authors
Fabio Sirchia, Eleonora Di Gregorio, Gabriella Restagno, Enrico Grosso, Patrizia Pappi, Flavia Talarico, Elisa Savin, Simona Cavalieri, Elisa Giorgio, Cecilia Mancini, Barbara Pasini, Jodhbir S. Mehta, Alfredo Brusco,