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A novel homozygous mutation of CFAP300 identified in a Chinese patient with primary ciliary dyskinesia and infertility

Primary ciliary dyskinesia (PCD) is a clinically rare, genetically and phenotypically heterogeneous condition characterized by chronic respiratory tract infections, male infertility, tympanitis, and laterality abnormalities. PCD is typically resulted from variants in genes encoding assembly or struc...

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Principais autores: Zheng Zhou, Qi Qi, Wen-Hua Wang, Jie Dong, Juan-Juan Xu, Yu-Ming Feng, Zhi-Chuan Zou, Li Chen, Jin-Zhao Ma, Bing Yao
Formato: Artigo
Idioma:Inglês
Publicado em: Wolters Kluwer Medknow Publications 2025-01-01
coleção:Asian Journal of Andrology
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Acesso em linha:https://journals.lww.com/10.4103/aja202477
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