Congenital Corneal Dystrophy
Author:
Publisher
American Medical Association (AMA)
Subject
Ophthalmology
Cited by 37 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Diagnostic yield of candidate genes in an Australian corneal dystrophy cohort;Molecular Genetics & Genomic Medicine;2022-08-19
2. Harboyan Syndrome: A Novel SLC4A11 Variant With Unique Genotype–Phenotype Correlation;Cornea;2022-04-08
3. Genetic profiles of non-syndromic severe-profound hearing loss in Chinese Hans by whole-exome sequencing;Gene;2022-04
4. SLC4A11 mutations causative of congenital hereditary endothelial dystrophy (CHED) progressing to Harboyan syndrome in consanguineous Pakistani families;Molecular Biology Reports;2021-10-12
5. Harboyan syndrome: novel SLC4A11 mutation, clinical manifestations, and outcome of corneal transplantation;Journal of Human Genetics;2020-09-03
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