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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Deafness and GIPC3[original query]
Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing.
Molecular genetics & genomic medicine 2015 May 3 (3): 189-96.
Ammar-Khodja Fatima, Bonnet Crystel, Dahmani Malika, Ouhab Sofiane, Lefèvre Gaelle M, Ibrahim Hassina, Hardelin Jean-Pierre, Weil Dominique, Louha Malek, Petit Christi
Targeted next generation sequencing reveals OTOF mutations in auditory neuropathy spectrum disorder.
International journal of pediatric otorhinolaryngology 2018 10 115 19-23.
Chen Kaitian, Liu Min, Wu Xuan, Zong Ling, Jiang Hongy
Low incidence of GIPC3 variants among the prelingual hearing impaired from southern India.
Journal of genetics 2020 11 99 .
Kalaimathi Murugesan, Subathra Mahalingam, Jeffrey Justin Margret, Selvakumari Mathiyalagan, Chandru Jayasankaran, Sharanya Narasimhan, Paridhy Vanniya S, Srisailapathy C R Srikuma
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