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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 - 7 (of 7 Records)

Query Trace: Disease and LOXHD1[original query]
[TGC Repeats in Intron 2 of the TCF4 Gene have a Good Predictive Power Regarding to Fuchs Endothelial Corneal Dystrophy].
Klinische Monatsblatter fur Augenheilkunde 2015 Aug .
Luther M, Grünauer-Kloevekorn C, Weidle E, Passarge E, Rupprecht A, Hoffmann K, Foja
Fine-Mapping of 18q21.1 Locus Identifies Single Nucleotide Polymorphisms Associated with Nonsyndromic Cleft Lip with or without Cleft Palate.
Frontiers in genetics 2016 7 88.
Mitra Amit K, Stessman Holly A F, Schaefer Robert J, Wang Wen, Myers Chad L, Van Ness Brian G, Beiraghi Sora
Analysis of candidate genes ZEB1 and LOXHD1 in late-onset Fuchs' endothelial corneal dystrophy in an Indian cohort.
Ophthalmic genetics 2018 May 1-7.
Rao Bhavna S, Ansar Samdani, Arokiasamy Tharigopala, Sudhir Rachapalli R, Umashankar Vetrivel, Rajagopal Rama, Soumittra Nagasa
A novel LOXHD1 variant in a Chinese couple with hearing loss.
The Journal of international medical research 2019 11 47 (12): 6082-6090.
Zhang Chuan, Hao Shengju, Liu Yali, Zhou Bingbo, Liu Furong, Zheng Lei, Ma Panpan, Liu Qing, Lin Xiaojuan, Yan Yousheng, Zhang Qingh
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome.
Journal of neurology 2021 1 268 (6): 2192-2207.
Chakrabarty Sanjiban, Govindaraj Periyasamy, Sankaran Bindu Parayil, Nagappa Madhu, Kabekkodu Shama Prasada, Jayaram Pradyumna, Mallya Sandeep, Deepha Sekar, Ponmalar J N Jessiena, Arivinda Hanumanthapura R, Meena Angamuthu Kanikannan, Jha Rajan Kumar, Sinha Sanjib, Gayathri Narayanappa, Taly Arun B, Thangaraj Kumarasamy, Satyamoorthy Kapaet
Genetic Analysis of the LOXHD1 Gene in Chinese Patients With Non-Syndromic Hearing Loss.
Frontiers in genetics 2022 6 13 825082.
Wang Wei-Qian, Gao Xue, Huang Sha-Sha, Kang Dong-Yang, Xu Jin-Cao, Yang Kun, Han Ming-Yu, Zhang Xin, Yang Su-Yan, Yuan Yong-Yi, Dai
Targeted next-generation sequencing analysis in Italian patients with keratoconus.
Eye (London, England) 2024 4 .
Marco Lombardo, Umberto Camellin, Raffaella Gioia, Sebastiano Serrao, Vincenzo Scorcia, Anna Maria Roszkowska, Giuseppe Lombardo, Matteo Bertelli, Maria Chiara Medori, Danilo Alunni Fegatelli, Annarita Vestri, Rita Mencucci, Domenico Schiano Lomoriel
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