Two novel mutations in a cystic fibrosis patient of Chinese origin-Reference-Cited by-同舟云学术

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Two novel mutations in a cystic fibrosis patient of Chinese origin

Published:1999-07-16 Issue:6 Volume:104 Page:511-515
ISSN:0340-6717
Container-title:Human Genetics
language:
Short-container-title:Human Genetics

Author:

Wagner John A.,Vassilakis Athina,Yee Kevin,Li Mei,Hurlock Gregory,Krouse Mauri E.,Moss Richard B.,Wine J. J.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s004390050996.pdf

Cited by 31 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetic analysis and functional study of novel CFTR variants in Chinese children with cystic fibrosis;Gene;2024-05

2. Loss-of-function CFTR p.G970D missense mutation might cause congenital bilateral absence of the vas deferens and be associated with impaired spermatogenesis;Asian Journal of Andrology;2023

3. Genetic spectrum of Chinese children with cystic fibrosis: comprehensive data analysis from the main referral centre in China;Journal of Medical Genetics;2022-07-20

4. A review of cystic fibrosis: Basic and clinical aspects;Animal Models and Experimental Medicine;2021-09

5. Pseudo‐Bartter syndrome in Chinese children with cystic fibrosis: Clinical features and genotypic findings;Pediatric Pulmonology;2020-08-13

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