Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Hearing Loss and MARVELD2[original query] |
---|
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 |
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 |
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 |
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 |
- Page last reviewed:Feb 1, 2024
- Page last updated:May 06, 2024
- Content source: