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Schnyder corneal dystrophy and associated phenotypes caused by novel and recurrent mutations in the UBIAD1 gene

Crossref DOI link: https://doi.org/10.1186/s12886-018-0918-8

Published Online: 2018-09-17

Published Print: 2018-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Evans, Cerys J.

Dudakova, Lubica

Skalicka, Pavlina

Mahelkova, Gabriela

Horinek, Ales

Hardcastle, Alison J.

Tuft, Stephen J.

Liskova, Petra
Funding

Funding for this research was provided by:

Univerzita Karlova v Praze (UNCE 204064, PROGRES-Q26/LF1, SVV 260367/2017, PROGRES Q25/LF1/2)

Grantová Agentura, Univerzita Karlova (GAUK 250361/2017)
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Article History

Received: 22 January 2018

Accepted: 6 September 2018

First Online: 17 September 2018

Ethics approval and consent to participate

: The study was approved by the Ethics committee of the General University Hospital in Prague (reference no. 151/11 S-IV) or Moorfields Eye Hospital (REC references 13/LO/1084 and 09/H0724/25). Written consent was obtained from all participants or their parents/legal guardians before inclusion.

: Not applicable.

: The authors declare that they have no competing interests.

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