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Nature Reviews. Genetics|May 12, 2023
Deafness: from genetic architecture to gene therapyChristine Petit, Crystel Bonnet, Saaïd SafieddineHuman Molecular Genetics|June 9, 2012
Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafnessSedigheh Delmaghani, Asadollah Aghaie, Nicolas Michalski, et al.Frontiers in Aging Neuroscience|March 18, 2021
Contributions of Age-Related and Audibility-Related Deficits to Aided Consonant Identification in Presbycusis: A Causal-Inference AnalysisLéo Varnet, Agnès C Léger, Sophie Boucher, et al.Vision Research|September 25, 2012
Fundus autofluorescence and optical coherence tomography in relation to visual function in Usher syndrome type 1 and 2Ana Fakin, Martina Jarc-Vidmar, Damjan Glavač, et al.International Journal of Pediatric Otorhinolaryngology|June 15, 2019
The spectrum of GJB2 gene mutations in Algerian families with nonsyndromic hearing loss from Sahara and Kabylie regionsSonia Talbi, Crystel Bonnet, Farid Boudjenah, et al.BMC Bioinformatics|April 15, 2021
Phylogenetic analysis of Harmonin homology domainsBaptiste Colcombet-Cazenave, Karen Druart, Crystel Bonnet, et al.Genes|December 11, 2019
Clinical and Haplotypic Variability of Slovenian USH2A Patients Homozygous for the c. 11864G>A Nonsense MutationAndrej Zupan, Ana Fakin, Saba Battelino, et al.International Journal of Pediatric Otorhinolaryngology|November 17, 2019
ATP6V1B1 recurrent mutations in Algerian deaf patients associated with renal tubular acidosisMalika Dahmani, Sonia Talbi, Fatima Ammar-Khodja, et al.Molecular Biology Reports|November 4, 2023
Novel pathogenic WHRN variant causing hearing loss in a moroccan familyImane AitRaise, Ghita Amalou, Salaheddine Redouane, et al.Molecular Biology Reports|July 25, 2024
Exome sequencing reveals pathogenic mutations in the LARS2 and HSD17B4 genes associated with Perrault syndrome and D-bifunctional protein deficiency in Moroccan familiesAssia Idyahia, Salaheddine Redouan, Ghita Amalou, et al.Pageof 23