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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

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Kun Xia

National Laboratory of Medical Genetics of China

Central South University

Changsha

Hunan

China

[email]@xysm.net

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Affiliation

National Laboratory of Medical Genetics of China, Central South University, Changsha, Hunan, China. 2004

References

A novel PRPF31 splice-site mutation in a Chinese family with autosomal dominant retinitis pigmentosa. Xia, K., Zheng, D., Pan, Q., Liu, Z., Xi, X., Hu, Z., Deng, H., Liu, X., Jiang, D., Deng, H., Xia, J. Mol. Vis. (2004) [Pubmed]
Mutation in PITX2 is associated with ring dermoid of the cornea. Xia, K., Wu, L., Liu, X., Xi, X., Liang, D., Zheng, D., Cai, F., Pan, Q., Long, Z., Dai, H., Hu, Z., Tang, B., Zhang, Z., Xia, J. J. Med. Genet. (2004) [Pubmed]