Highly efficient, label free, ultrafast plasmonic SERS biosensor (silver nanoarrays/Si) to detect GJB2 gene expressed deafness mutations in real time validated with PCR studies
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Elsevier BV
Reference32 articles.
1. Prevalence of hearing impairment and outcome of universal neonatal hearing screening program in a tertiary care hospital–in UAE;ElHalik;J Pediatr Neonatal Care,2021
2. Whole exome sequencing, in silico and functional studies confirm the association of the GJB2 mutation p. Cys169Tyr with deafness and suggest a role for the TMEM59 gene in the hearing process;Mahfood;Saudi journal of biological sciences,2021
3. Genetics of hereditary hearing loss in the Middle East: A systematic review of the carrier frequency of the GJB2 mutation (35delG);Koohiyan;Audiology and Neurotology,2019
4. Whole-exome sequencing efficiently detects rare mutations in autosomal recessive nonsyndromic hearing loss;Diaz-Horta;PloS One,2012
5. Identification of a novel frameshift mutation in the ILDR1 gene in a UAE family, mutations review and phenotype genotype correlation;Tlili;PloS One,2017
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