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Paper published by Dr Xiaoyun Hu:
Case report
Identification of a Novel VPS13B Mutation in a Chinese Patient with Cohen Syndrome by Whole-Exome Sequencing
Hu X, Huang T, Liu Y, Zhang L, Zhu L, Peng X, Zhang S
Pharmacogenomics and Personalized Medicine 2021, 14:1583-1589
Published Date: 4 December 2021