Disease-associated variants of Gap Junction Beta 2 protein (GJB2) in the deaf population of Southern Punjab of Pakistan. [PDF]
PLoS One, 2021 Kausar N +7 more
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Identification of homozygous missense variant in SIX5 gene underlying recessive nonsyndromic hearing impairment. [PDF]
PLoS One, 2022 Kakar MU +10 more
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There Is More Than Meets the Eye: Identification of Dual Molecular Diagnosis in Patients Affected by Hearing Loss. [PDF]
Biomedicines, 2021 Morgan A +7 more
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The Genomics of Auditory Function and Disease. [PDF]
Annu Rev Genomics Hum Genet, 2022 Taiber S +3 more
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Tendon and Ligament Genetics: How Do They Contribute to Disease and Injury? A Narrative Review. [PDF]
Life (Basel), 2022 Ribbans WJ, September AV, Collins M.
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Identification and phased de novo mutation of the EPS8L2 gene in a patient with progressive hearing loss: A case report. [PDF]
Medicine (Baltimore)Gan H +9 more
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Genes linked to hearing and vestibular phenotypes in humans and mice: an interspecies systematic review. [PDF]
Hum GenomicsAyoub C +3 more
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Genetic and Environmental Factors Shaping Hearing Loss: Xenobiotics, Mechanisms and Translational Perspectives. [PDF]
J XenobiotEsteves F, Caria H.
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Evaluation of the GJB2 and GJB6 Polymorphisms with Autosomal Recessive Nonsyndromic Hearing Loss in Iranian Population. [PDF]
Iran J Otorhinolaryngol, 2021 Ebrahimkhani S, Asaadi Tehrani G.
europepmc +1 more source
A Rare Mutation in the MARVELD2 Gene Can Cause Nonsyndromic Hearing Loss. [PDF]
Int Med Case Rep J, 2020 Sadeghi Z +4 more
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