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Presentation of potential genes and deleterious variants associated with non-syndromic hearing loss: a computational approach
Manisha Ray, Surya Narayan Rath, Saurav Sarkar, Mukund Namdev Sable
Genomics Inform. 2022;20(1):e5  Published online March 31, 2022
DOI: https://doi.org/10.5808/gi.21070

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Presentation of potential genes and deleterious variants associated with non-syndromic hearing loss: a computational approach
Genomics & Informatics. 2022;20(1):e5   Crossref logo
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Comprehensive functional network analysis and screening of deleterious pathogenic variants in non-syndromic hearing loss causative genes
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Variants in CDH23 Cause Broad Spectrum of Hearing Loss: From Non-Syndromic to Syndromic Hearing Loss as Well as From Congenital to Age-Related Hearing Loss
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Views of healthcare professionals on the inclusion of genes associated with non-syndromic hearing loss in reproductive genetic carrier screening
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Prediction of deleterious non-synonymous SNPs of human TLR2 gene associated with bacterial meningitis and hearing impairment by computational approach
International journal of health sciences. 2022;3735-3749   Crossref logo
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Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden
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Lights and Shadows in the Genetics of Syndromic and Non-Syndromic Hearing Loss in the Italian Population
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Variants in CDH23 cause a broad spectrum of hearing loss: from non-syndromic to syndromic hearing loss as well as from congenital to age-related hearing loss
Human Genetics. 2022;141(3-4):903-914   Crossref logo
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Non-syndromic hereditary sensorineural hearing loss: review of the genes involved
The Journal of Laryngology & Otology. 2014;128(1):13-21   Crossref logo
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The Promise of Whole-Exome Sequencing in Detecting Novel Variants of the MYO15A Gene in Two Iranian Pedigrees with Non-Syndromic Hearing Loss, A descriptive experimental study
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