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

Authors

  • Vilavun Puangsricharern Faculty of Medicine, Department of Ophthalmology, Chulalongkorn University, Bangkok, Thailand Center of Excellence for Cornea and Limbal Stem Cell Transplantation, King Chulalongkorn Memorial Hospital, the Thai Red Cross Society, Bangkok, Thailand PubMed articlesGoogle scholar articles
  • Patra Yeetong Faculty of Science, Department of Botany, Chulalongkorn University, Bangkok, Thailand PubMed articlesGoogle scholar articles
  • Chonthicha Charumalai Faculty of Medicine, Department of Ophthalmology, Chulalongkorn University, Bangkok, Thailand PubMed articlesGoogle scholar articles
  • Kanya Suphapeetiporn Faculty of Medicine, Department of Pediatrics, Center of Excellence for Medical Genetics, Chulalongkorn University, Bangkok, Thailand Center of Excellence for Medical Genetics, King Chulalongkorn Memorial Hospital, the Thai Red Cross Society, Bangkok, Thailand PubMed articlesGoogle scholar articles
  • Vorasuk Shotelersuk Faculty of Medicine, Department of Pediatrics, Center of Excellence for Medical Genetics, Chulalongkorn University, Bangkok, Thailand Center of Excellence for Medical Genetics, King Chulalongkorn Memorial Hospital, the Thai Red Cross Society, Bangkok, Thailand PubMed articlesGoogle scholar articles
  1. Correspondence to Professor Kanya Suphapeetiporn, Division of Medical Genetics and Metabolism, Department of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand; kanya.su{at}chula.ac.th
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Citation

Puangsricharern V, Yeetong P, Charumalai C, et al
Two novel mutations including a large deletion of the SLC4A11 gene causing autosomal recessive hereditary endothelial dystrophy

Publication history

  • Received May 24, 2014
  • Revised July 11, 2014
  • Accepted July 26, 2014
  • First published August 19, 2014.
Online issue publication 
March 22, 2016

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