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About this Biochemistry, Genetics and Molecular Biology article
Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locus by Chen, W. (author);Kahrizi, K. (author);Meyer, N. C. (author);Riazalhosseini, Y. (author);Van Camp, G. (author);Najmabadi, H. (author);Smith, R. J. (author) is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- Chen, W. (author);Kahrizi, K. (author);Meyer, N. C. (author);Riazalhosseini, Y. (author);Van Camp, G. (author);Najmabadi, H. (author);Smith, R. J. (author)
- Publisher
- BMJ Publishing Group; BMJ (ISSN 0022-2593)
- Published
- 2005
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)