Absence of phenotype-genotype correlation of patients expressing mutations in the SLC4A11 gene

• Main Authors: Mehta, J.S., Tan, D.T., Aung, T., Vithana, E.N., Hemadevi, B., Sundaresan, P., Arunkumar, J., Srinivasan, M., Prajna, V.
• Other Authors: OPHTHALMOLOGY
• Format: Review
• Published: 2011
• Subjects: CHED; Harboyan Syndrome; PCR; Penetrating Keratoplasty; SLC4A11
• Online Access: http://scholarbank.nus.edu.sg/handle/10635/26567
• Institution: National University of Singapore

10.1097/ICO.0b013e3181ae9038