Novel deletion mutations of the PIH1D3 gene in an infertile young man with primary ciliary dyskinesia and his cousin with Kartagener's syndrome

Detalles Bibliográficos
Autores principales: Huang, Chuan, Liu, Na-Chuan, Wang, Xiao-Bo, Gu, Ben-Hong, Zhang, Jian-Xiong, Li-Zhang, Li, Zheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
Materias:
Letter to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152414/
https://www.ncbi.nlm.nih.gov/pubmed/33106461
http://dx.doi.org/10.4103/aja.aja_43_20

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