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Query Trace: Hearing Loss and MARVELD2[original query]

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 Similar articles in PubMed
Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss. PloS one 2015 10 (11): e0142154. Atik Tahir, Onay Huseyin, Aykut Ayca, Bademci Guney, Kirazli Tayfun, Tekin Mustafa, Ozkinay Fer Similar articles in PubMed
MARVELD2 (DFNB49) mutations in the hearing impaired Central European Roma population--prevalence, clinical impact and the common origin. PloS one 2015 10 (4): e0124232. Mašindová Ivica, Šoltýsová Andrea, Varga Lukáš, Mátyás Petra, Ficek Andrej, Hu?ková Miloslava, S?rová Martina, Šafka-Brožková Dana, Anwar Saima, Bene Judit, Straka Slavomír, Janicsek Ingrid, Ahmed Zubair M, Seeman Pavel, Melegh Béla, Profant Milan, Klimeš Iwar, Riazuddin Saima, Kádasi ?udevít, Gašperíková Danie Similar articles in PubMed
New SNP variants of MARVELD2 (DFNB49) associated with non-syndromic hearing loss in Chinese population. Journal of Zhejiang University. Science. B 0 20 (2): 164-169. Zheng Jing, Meng Wen-Fang, Zhang Chao-Fan, Liu Han-Qing, Yao Juan, Wang Hui, Chen Ye, Guan Min-X Similar articles in PubMed