Xin-Fu Lin
3PUBLICATIONS
19CO-AUTHORS
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Publications (3)
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|May 09, 2022
Analysis of a Family with Brugada Syndrome and Sudden Cardiac Death Caused by a Novel Mutation of SCN5A.Yao-Bin Zhu, Jian-Hui Zhang, Yuan-Yuan Ji
|Nov 16, 2021
Different phenotypes of neurological diseases, including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism, caused by de novo ATP1A3 mutation in a family.Wen Wei, Xiu-Fen Zheng, Dan-Dan Ruan
|May 28, 2021
Review and Analysis of Two Gitelman Syndrome Pedigrees Complicated with Proteinuria or Hashimoto's Thyroiditis Caused by Compound Heterozygous SLC12A3 Mutations.Jian-Hui Zhang, Dan-Dan Ruan, Ya-Nan Hu
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Frequent Collaborators
3 joint publications
Dan-Dan Ruan
3 joint publications
Jie-Wei Luo
2 joint publications
Jian-Hui Zhang
2 joint publications
Ya-Nan Hu
2 joint publications
Yao-Bin Zhu
2 joint publications
Fa-Qiang Tang
1 joint publications
Xing-Lin Ruan
1 joint publications
Xiao Yang
1 joint publications
Jia-Bin Wu
1 joint publications
Wen Wei
