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Article

Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees.

BMC medical genetics - 18 Nov 2020

Khatami Somayeh, Askari Masomeh, Bahreini Fatemeh, Hashemzadeh-Chaleshtori Morteza, Hematian Saeed, Asgharzade Samira

Abstract excerpt

BACKGROUND: Clinical genetic diagnosis of non-syndromic hearing loss (NSHL) is quite challenging. With regard to its high heterogeneity as well as large size of some genes, it is also really difficult to detect causative mutations using traditional approaches. One of the recent technologies called whole-exome sequencing (WES) has been thus developed in this domain to remove the limitations of conventional...

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Identifiers

PMID: 33208113
DOI: 10.1186/s12881-020-01168-x
PMCID: PMC7672957

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Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees.PMID 33208113Read ↗

Novel MYO15A Variants are Associated with Hearing Loss in the Two Iranian PedigreesSemantic proximity Read ↗

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