Xihui Chen
4PUBLICATIONS
1CO-AUTHORS
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Publications (4)
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|Aug 20, 2022
TFG mutation induces haploinsufficiency and drives axonal Charcot-Marie-Tooth disease by causing neurite degeneration.Xihui Chen, Fangfang Liu, Kun Chen
|Dec 30, 2020
Novel mutations in hyper-IgM syndrome type 2 and X-linked agammaglobulinemia detected in three patients with primary immunodeficiency disease.Xihui Chen, Fangfang Liu, Lijuan Yuan
|Jun 15, 2019
Mutational Analysis of TYR, OCA2, and SLC45A2 Genes in Chinese Families with Oculocutaneous Albinism.Ye Lin, Xihui Chen, Ying Yang
|Jan 10, 2018
Two novel CPS1 mutations in a case of carbamoyl phosphate synthetase 1 deficiency causing hyperammonemia and leukodystrophy.Xihui Chen, Lijuan Yuan, Mao Sun
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