A Novel Compound Heterozygous Mutation in the DNAH11 Gene Found in Neonatal Twins With Primary Ciliary Dyskinesis

Background: Primary ciliary dyskinesia (PCD) is a rare genetically heterogeneous disorder of motile cilia. Common features of PCD include upper and lower respiratory tract disease, secretory otitis media, situs inversus and fertility problems. To date, although several PCD-associated genes have been...

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Detalles Bibliográficos
Autores principales: Dong, Shumei, Bei, Fei, Yu, Tingting, Sun, Luming, Chen, Xiafang, Yan, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8919259/
https://www.ncbi.nlm.nih.gov/pubmed/35295944
http://dx.doi.org/10.3389/fgene.2022.814511

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8919259/
https://www.ncbi.nlm.nih.gov/pubmed/35295944
http://dx.doi.org/10.3389/fgene.2022.814511

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