Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Hearing and CLDN14[original query] |
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Mutation in gap and tight junctions in patients with non-syndromic hearing loss. Biochemical and biophysical research communications 2009 Jul 385 (1): 1-5. Belguith Hanen, Tlili Abedelaziz, Dhouib Houria, Ben Rebeh Imen, Lahmar Imed, Charfeddine Ilhem, Driss Nabil, Ghorbel Abdelmonem, Ayadi Hammadi, Masmoudi Sab |
Genetic analysis of genes related to tight junction function in the Korean population with non-syndromic hearing loss. PloS one 2014 9 (4): e95646. Kim Min-A, Kim Ye-Ri, Sagong Borum, Cho Hyun-Ju, Bae Jae Woong, Kim Jeongho, Lee Jinwook, Park Hong-Joon, Choi Jae Young, Lee Kyu-Yup, Kim Un-Kyu |
Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome. Clinical genetics 2016 Sep . Faridi Rabia, Rehman Atteeq U, Morell Robert J, Friedman Penelope L, Demain Leigh, Zahra Sana, Khan Asma Ali, Tohlob Dalia, Assir Muhammad Zaman, Beaman Glenda, Khan Shaheen N, Newman William G, Riazuddin Sheikh, Friedman Thomas |
A common variant in CLDN14 causes precipitous, prelingual sensorineural hearing loss in multiple families due to founder effect. Human genetics 2016 Nov . Pater Justin A, Benteau Tammy, Griffin Anne, Penney Cindy, Stanton Susan G, Predham Sarah, Kielley Bernadine, Squires Jessica, Zhou Jiayi, Li Quan, Abdelfatah Nelly, O'Rielly Darren D, Young Terry-Ly |
Genetic analysis of CLDN14 in the Chinese population affected with non-syndromic hearing loss. International journal of pediatric otorhinolaryngology 2018 2 105 6-11. Lu Yajie, Yao Jun, Wei Qinjun, Xu Jin, Xing Guangqian, Cao X |
Detailed Clinical Features of Deafness Caused by a Claudin-14 Variant. International journal of molecular sciences 2019 9 20 (18): . Kitano Tomohiro, Kitajiri Shin-Ichiro, Nishio Shin-Ya, Usami Shin-Ic |
Excess of Rare Missense Variants in Hearing Loss Genes in Sporadic Meniere Disease. Frontiers in genetics 2019 10 76. Gallego-Martinez Alvaro, Requena Teresa, Roman-Naranjo Pablo, Lopez-Escamez Jose |
A Novel Nonsense Mutation (c.414G>A; p.Trp138*) in CLDN14 Causes Hearing Loss in Yemeni Families: A Case Report. Frontiers in genetics 2019 11 10 1087. Mohamed Walaa Kamal Eldin, Mahfood Mona, Al Mutery Abdullah, Abdallah Sallam Hasan, Tlili Abdelaz |
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- Page last updated:Mar 25, 2024
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