Dan-Dan Ruan
4PUBLICATIONS
25CO-AUTHORS
Get your video featured.
Publish with JoVEGet your video featured.
Publish with JoVE
Publications (4)
Sort by Publication Date:
|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
|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
Pageof 1
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
