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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 24, 2023. (Total: 221393Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Deafness and DFNB31[original query]
Sequence variants of the DFNB31 gene among Usher syndrome patients of diverse origin.
Molecular vision 2010 16 495-500.
Aller Elena, Jaijo Teresa, van Wijk Erwin, Ebermann Inga, Kersten Ferry, García-García Gema, Voesenek Krysta, Aparisi María José, Hoefsloot Lies, Cremers Cor, Díaz-Llopis Manuel, Pennings Ronald, Bolz Hanno J, Kremer Hannie, Millán José
Comprehensive molecular diagnosis of 67 Chinese Usher syndrome probands: high rate of ethnicity specific mutations in Chinese USH patients.
Orphanet journal of rare diseases 2015 10 (1): 110.
Jiang Lichun, Liang Xiaofang, Li Yumei, Wang Jing, Zaneveld Jacques Eric, Wang Hui, Xu Shan, Wang Keqing, Wang Binbin, Chen Rui, Sui Ruifa
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
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