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Dan-Dan Ruan

4PUBLICATIONS
25CO-AUTHORS
Gene mappingNeurology and neuromuscular diseasesGenomicsPredictive and prognostic markers
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Publications (4)

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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

|May 06, 2021
Mutational Analysis of a Familial Adenomatous Polyposis Pedigree with Bile Duct Polyp Phenotype.

Li-Jun Xie, Dan-Dan Ruan, Jian-Hui Zhang

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Frequent Collaborators

4 joint publications

Jie-Wei Luo

3 joint publications

Jian-Hui Zhang

3 joint publications

Xin-Fu Lin

2 joint publications

Fa-Qiang Tang

2 joint publications

Ya-Nan Hu

2 joint publications

Yao-Bin Zhu

1 joint publications

Li-Jun Xie

1 joint publications

Yi Li

1 joint publications

Wei Chen

1 joint publications

Mao-Lin Yan

Frequent Collaborators

4 joint publications

Jie-Wei Luo

3 joint publications

Jian-Hui Zhang

3 joint publications

Xin-Fu Lin

2 joint publications

Fa-Qiang Tang

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