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K Xia

First name:
K
Last name:
Xia
Yin, X., Lin, J., Cao, L., Zhang, T., Zeng, S., Zhang, K., … Tang, B. (2018). Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene. Human Molecular Genetics. https://doi.org/10.1093/hmg/ddy025 (Original work published 2018)
Zou, Y., He, W., Wang, K., Han, H., Xiao, T., Chen, X., … Zhang, Z. (2018). Identification of rare RTN3 variants in Alzheimer’s disease in Han Chinese. Human Genetics. https://doi.org/10.1007/s00439-018-1868-1 (Original work published 2018)
Pakhrin, P., Xie, Y., Hu, Z., Li, X., Liu, L., Huang, S., … Zhang, R. (2018). Genotype-phenotype correlation and frequency of distribution in a cohort of Chinese Charcot-Marie-Tooth patients associated with GDAP1 mutations. Journal of Neurology. https://doi.org/10.1007/s00415-018-8743-9 (Original work published 2018)