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Congenital hereditary endothelial dystrophy with progressive sensorineural deafness: a case report of Harboyan syndrome.
Harboyan syndrome with biallelic SLC4A11 pathogenic variants misdiagnosed as congenital CMV infection.
Harboyan Syndrome: A Novel SLC4A11 Variant With Unique Genotype-Phenotype Correlation.
SLC4A11 mutations causative of congenital hereditary endothelial dystrophy (CHED) progressing to Harboyan syndrome in consanguineous Pakistani families.
Harboyan Syndrome.