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

Novel deletion mutations of the PIH1D3 gene in an infertile young man with primary ciliary dyskinesia and his cousin with Kartagener's syndrome.
Asian J Androl. 2020 Oct 20;:
Authors: Huang C, Liu NC, Wang XB, Gu BH, Zhang JX, Li-Zhang, Li Z
PMID: 33106461 [PubMed - as supplied by publisher]

Source: Asian Journal of Andrology - October 20, 2020 Category: Urology & Nephrology Authors: Huang C, Liu NC, Wang XB, Gu BH, Zhang JX, Li-Zhang, Li Z Tags: Asian J Androl Source Type: research