Associated Papers
DALIA- a comprehensive resource of Disease Alleles in Arab population.
Vatsyayan A et al.
Plos One, 2021
33439861 (PubMed )
Supplement: pone.0244567.s011.xlsx › Sheet1
Analysis of CLDN14 gene in deaf Moroccan patients with non-syndromic hearing loss.
Charif M et al.
Gene, 2013
Genetic and molecular analysis of the CLDN14 gene in Moroccan family with non-syndromic hearing loss.
Charif M et al.
Indian Journal of Human Genetics, 2013
tSNP-based identification of allelic loss of gene expression in a patient with a balanced chromosomal rearrangement.
Guzauskas GF et al.
Genomics, 2007
Different mechanisms preclude mutant CLDN14 proteins from forming tight junctions in vitro.
Wattenhofer M et al.
Human Mutation, 2005
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