Whole-exome sequencing identification of novel DNAH5 mutations in a young patient with primary ciliary dyskinesia-Reference-Cited by-同舟云学术

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Whole-exome sequencing identification of novel DNAH5 mutations in a young patient with primary ciliary dyskinesia

Published:2016-10-21 Issue:6 Volume:14 Page:5077-5083
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:en
Short-container-title:

Author:

Kano Gen,Tsujii Hisashi,Takeuchi Kazuhiko,Nakatani Kaname,Ikejiri Makoto,Ogawa Satoru,Kubo Hisami,Nagao Mizuho,Fujisawa Takao

Publisher

Spandidos Publications

Subject

Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Cited by 18 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. Diagnosis of Primary Ciliary Dyskinesia via Whole Exome Sequencing and Histologic Findings;Yonsei Medical Journal;2024

2. Dual-allele heterozygous mutation of DNAH5 gene in a boy with primary ciliary dyskinesia: A case report;Medicine;2023-12-29

3. Cystic fibrosis and primary ciliary dyskinesia: Similarities and differences;Respiratory Medicine;2023-04

4. Characteristic genetic spectrum of primary ciliary dyskinesia in Japanese patients and global ethnic heterogeneity: population-based genomic variation database analysis;Journal of Human Genetics;2023-03-02

5. A whole-exome analysis of non-syndromic hearing loss patients from India reveals a wide spectrum of known and novel mutations;2023-02-10

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