Whole exome sequencing identified a pathogenic nonsense mutation in LMNA in a family with a progressive cardiac conduction defect: A case report.
| Autor: | PENG FAN1, DI ZHANG2, KUN-QI YANG1, TAO TIAN1, FANG LUO1, YA-XIN LIU2, LIN-PING WANG1 wanglping@139.com, XIAN-LIANG ZHOU1 |
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| Zdroj: | Molecular Medicine Reports. Jun2020, Vol. 21 Issue 6, p2459-2465. 7p. |
| Databáze: | Academic Search Ultimate |
| Externí odkaz: |
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