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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 - 6 (of 6 Records)

Query Trace: Disease and OTOF[original query]
Screening of DFNB3 in Iranian families with autosomal recessive non-syndromic hearing loss reveals a novel pathogenic mutation in the MyTh4 domain of the MYO15A gene in a linked family.
Iranian journal of basic medical sciences 2016 Jul 19 (7): 772-8.
Reiisi Somayeh, Tabatabaiefar Mohammad Amin, Sanati Mohammad Hosein, Chaleshtori Morteza Hashemzad
Genetic Susceptibility Study of Chinese Sudden Sensorineural Hearing Loss Patients with Vertigo.
Current medical science 2021 Aug 41 (4): 673-679.
Gao Yun, Wang Hong-Yang, Guan Jing, Lan Lan, Zhao Cui, Xie Lin-Yi, Wang Da-Yong, Wang Qiu-
Whole-Exome Sequencing Reveals a Rare Variant of OTOF Gene Causing Congenital Non-syndromic Hearing Loss Among Large Muslim Families Favoring Consanguinity.
Frontiers in genetics 2021 6 12 641925.
Fareed Mohd, Sharma Varun, Singh Inderpal, Rehman Sayeed Ur, Singh Gurdarshan, Afzal Mohamm
Genetic etiological analysis of auditory neuropathy spectrum disorder by next-generation sequencing.
Frontiers in neurology 2022 12 13 1026695.
Sun Lianhua, Lin Zhengyu, Zhang Jifang, Shen Jiali, Wang Xiaowen, Yang J
Effects of copy number variations on longevity in late-onset Alzheimer's disease patients: insights from a causality network analysis.
Frontiers in aging neuroscience 2023 11 15 1241412.
Yanan Hao, Chuhao Li, He Wang, Chen Mi
Whole Exome Sequencing of Non-Syndromic Hearing Loss Patients.
Iranian journal of public health 2024 6 53 (2): 453-461.
Hossein Naddafnia, Zahra Noormohammadi, Shiva Irani, Iman Salahshoorif
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