Novel Phenotype-Genotype Correlations of Restrictive Cardiomyopathy With Myosin-Binding Protein C (MYBPC3) Gene Mutations Tested by Next-Generation Sequencing.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Works matching AU Lu, Chao-Xia
Results: 4
1
2
A novel frameshift mutation of epithelial sodium channel β-subunit leads to Liddle syndrome in an isolated case.
- Published in:
- Clinical Endocrinology, 2015, v. 82, n. 4, p. 611, doi. 10.1111/cen.12650
- By:
- Publication type:
- Article
3
Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome.
- Published in:
- Clinical & Experimental Hypertension, 2018, v. 40, n. 2, p. 107, doi. 10.1080/10641963.2017.1334799
- By:
- Publication type:
- Article
4
Truncated Epithelial Sodium Channel β Subunit Responsible for Liddle Syndrome in a Chinese Family.
- Published in:
- Kidney & Blood Pressure Research, 2019, v. 44, n. 5, p. 942, doi. 10.1159/000500919
- By:
- Publication type:
- Article