Publications:

Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders.

Human Reproduction (Oxford, England)

Oud, M S MS; Houston, B J BJ; Volozonoka, L L; Mastrorosa, F K FK; Holt, G S GS; Alobaidi, B K S BKS; deVries, P F PF; Astuti, G G; Ramos, L L; Mclachlan, R I RI; O'Bryan, M K MK; Veltman, J A JA; Chemes, H E HE; Sheth, H H

Publication Date: 2021-08-18

Variant appearance in text: PKD1: 917A>G

PubMed Link: 34089056

Variant Present in the following documents:

• deab099_supplementary_tables3.pdf

View BVdb publication page