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Two novel mutations including a large deletion of the SLC4A11 gene causing autosomal recessive hereditary endothelial dystrophy

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  • VP and PY contributed equally.

  • Contributors VP collected the data, helped with interpretation of histological data and drafted the manuscript. PY performed molecular studies, analysed the data and drafted the manuscript. CC collected the data and helped with analysis of the images. KS and VS designed the study, undertook data analysis and interpretation and wrote the manuscript.

  • Funding This work was supported by the Ratchadapiseksomphot Endowment Fund of Chulalongkorn University (RES560530177-HR) and Thailand Research Fund.

  • Competing interests None.

  • Patient consent Obtained.

  • Ethics approval The institutional review board of the Faculty of Medicine of Chulalongkorn University.

  • Provenance and peer review Not commissioned; externally peer reviewed.