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Xin-Fu Lin

3PUBLICATIONS

19CO-AUTHORS

Gene mappingNeurology and neuromuscular diseasesGenomics

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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 <i>SLC12A3</i> 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

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

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