Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss

BACKGROUND: Hereditary hearing loss (HL) is a heterogeneous and most common sensory neural disorder. At least, 76 genes have been reported in association with autosomal recessive nonsyndromic HL (ARNSHL). Herein, we subjected two patients with bilateral sensorineural HL in two distinct consanguineou...

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Bibliografiset tiedot
Julkaisussa:Mol Genet Genomic Med
Päätekijät: Zardadi, Safoura, Razmara, Ehsan, Asgaritarghi, Golareh, Jafarinia, Ehsan, Bitarafan, Fatemeh, Rayat, Sima, Almadani, Navid, Morovvati, Saeid, Garshasbi, Masoud
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: John Wiley and Sons Inc. 2020
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Original Articles
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7767568/
https://ncbi.nlm.nih.gov/pubmed/33205915
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.1550
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