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Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset Hypertension. [electronic resource] by
- Fan, Peng
- Pan, Xiao-Cheng
- Zhang, Di
- Yang, Kun-Qi
- Zhang, Ying
- Tian, Tao
- Luo, Fang
- Ma, Wen-Jun
- Liu, Ya-Xin
- Wang, Lin-Ping
- Zhang, Hui-Min
- Song, Lei
- Cai, Jun
- Zhou, Xian-Liang
Producer: 20210712
In:
American journal of hypertension vol. 33
Availability: No items available.
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Genetic diagnosis of Liddle's syndrome by mutation analysis of SCNN1B and SCNN1G in a Chinese family. [electronic resource] by
- Wang, Lin-ping
- Gao, Ling-gen
- Zhou, Xian-liang
- Wu, Hai-ying
- Zhang, Lin
- Wen, Dan
- Li, Yue-hua
- Liu, Ya-xin
- Tian, Tao
- Fan, Xiao-han
- Jiang, Xiong-Jing
- Zhang, Hui-min
- Hui, Ru-tai
Producer: 20120918
In:
Chinese medical journal vol. 125
Availability: No items available.
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