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- [21] Whole-exome sequencing identifies a novel CCDC151 mutation, c.325G>T (p.E109X), in a patient with primary ciliary dyskinesia and situs inversus Journal of Human Genetics, 2019, 64 : 249 - 252
- [23] Correction: Whole-exome sequencing identifies a novel CCDC151 mutation, c.325GT (p.E109X), in a patient with primary ciliary dyskinesia and situs inversus Journal of Human Genetics, 2019, 64 : 829 - 829