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Whole exome sequencing enhances diagnosis of hereditary bronchiectasis.

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Title: Whole exome sequencing enhances diagnosis of hereditary bronchiectasis.
Authors: Zhou, Wangji1,2 (AUTHOR), Li, Yixuan3 (AUTHOR), Zheng, Haixia4 (AUTHOR), He, Miao4 (AUTHOR), Zhang, Miaoyan1 (AUTHOR), Chen, Qiaoling1 (AUTHOR), Situ, Christopher5 (AUTHOR), Wang, Yaqi1 (AUTHOR), Zhang, Ting1 (AUTHOR), Chen, Keqi1 (AUTHOR), Dai, Jinrong1 (AUTHOR), Meng, Shuzhen1 (AUTHOR), Liu, Xueqi1 (AUTHOR), Wu, Aohua1 (AUTHOR), Liu, Yaping3 (AUTHOR) ypliu_pumc@163.com, Xu, Kai-Feng1 (AUTHOR), Tian, Xinlun1,2 (AUTHOR) xinlun_t@sina.com, Zhang, Xue4 (AUTHOR)
Source: Orphanet Journal of Rare Diseases. 3/24/2025, Vol. 20 Issue 1, p1-8. 8p.
Database: Academic Search Ultimate
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ISSN:17501172
DOI:10.1186/s13023-025-03661-z