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About this Biochemistry, Genetics and Molecular Biology article
Novel truncation mutations in MYRF cause autosomal dominant high hyperopia mapped to 11p12–q13.3 by Xiao, Xueshan ;Sun, Wenmin ;Ouyang, Jiamin ;Li, Shiqiang ;Jia, Xiaoyun ;Tan, Zhiqun ;Hejtmancik, J. Fielding ;Zhang, Qingjiong 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
- Xiao, Xueshan ;Sun, Wenmin ;Ouyang, Jiamin ;Li, Shiqiang ;Jia, Xiaoyun ;Tan, Zhiqun ;Hejtmancik, J. Fielding ;Zhang, Qingjiong
- Publisher
- Springer; Springer-Verlag; Springer Verlag; Springer Science and Business Media LLC; Society for Mining, Metallurgy and Exploration Inc. (ISSN 0340-6717)
- Published
- 2019
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)