Molecular screening of patients with nonsyndromic hearing loss from Nanjing city of China

Author:

Lu Yajie,Dai Dachun,Chen Zhibin,Cao Xin,Bu Xingkuan,Wei Qinjun,Xing Guangqian

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Reference50 articles.

1. Epidermiology, etiology and ge-netic patterns;Cohen,1995

2. Hereditary deafness and phenotyping in humans;Bitner-Glindzicz;Br Med Bull,2002

3. Prevalent connexin 26 gene (GJB2) mutations in Japanese;Abe;J Med Genet,2000

4. Mitochondrial deafness;Fischel-Ghodsian;Ear Hear,2003

5. Screening of 38 genes identifies mutations in 62% of families with nonsyndromic deafness in Turkey;Duman;Genet Test Mol Biomarkers,2011

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