| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5589284 | Gene | 2017 | 39 Pages |
Abstract
The comprehensive methods may be useful in distinguishing the pathogenic mutations from the variations in PKD1, PKD2 and PKHD1 genes for prenatal diagnosis and presymptom diagnosis of PKD. Our results also enriched PKD genes mutation spectrum and evolved possible genotype-phenotype correlations of Chinese Han population.
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Related Topics
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Biochemistry, Genetics and Molecular Biology
Genetics
Authors
Zishui Fang, Shiyan Xu, Yonghua Wang, Liwei Sun, Yi Feng, Yibin Guo, Hongyi Li, Weiying Jiang,