Identification of compound heterozygous DNAH11 variants in a Han‐Chinese family with primary ciliary dyskinesia-Reference-Cited by-同舟云学术

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Identification of compound heterozygous DNAH11 variants in a Han‐Chinese family with primary ciliary dyskinesia

Published:2021-08-18 Issue:18 Volume:25 Page:9028-9037
ISSN:1582-1838
Container-title:Journal of Cellular and Molecular Medicine
language:en
Short-container-title:J Cell Mol Med

Author:

Xiong Ying¹,Xia Hong¹²,Yuan Lamei¹³,Deng Sheng¹⁴,Ding Zerui¹,Deng Hao¹³⁵^ORCID

Affiliation:

1. Center for Experimental Medicine The Third Xiangya Hospital Central South University Changsha China

2. Department of Emergency The Third Xiangya Hospital Central South University Changsha China

3. Disease Genome Research Center Central South University Changsha China

4. Department of Pharmacy Xiangya Hospital Central South University Changsha China

5. Department of Neurology The Third Xiangya Hospital Central South University Changsha China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Cell Biology,Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jcmm.16866

Reference57 articles.

1. Primary Ciliary Dyskinesia. Recent Advances in Diagnostics, Genetics, and Characterization of Clinical Disease

2. Recent advances in primary ciliary dyskinesia

3. European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia

4. Advances in the Genetics of Primary Ciliary Dyskinesia

5. Primary Ciliary Dyskinesia: An Update on Clinical Aspects, Genetics, Diagnosis, and Future Treatment Strategies

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3. Transmission disequilibrium analysis of whole genome data in childhood-onset systemic lupus erythematosus;Genes & Immunity;2023-07-24

4. Identification of novel compound heterozygous variants in the DNAH1 gene of a Chinese family with left-right asymmetry disorder;Frontiers in Molecular Biosciences;2023-06-29

5. Novel compound heterozygous variants in the USH2A gene associated with autosomal recessive retinitis pigmentosa without hearing loss;Frontiers in Cell and Developmental Biology;2023-02-15

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