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ABSTRACT: Purpose
To evaluate the unknown genetic causes of teratozoospermia, and determine the pathogenicity of candidate variants.Methods
A primary infertile patient and his family members were recruited in the West China Second University Hospital of Sichuan University. Whole-exome sequencing was performed to identify causative genes in a man with teratozoospermia. Immunofluorescence staining and western blotting were applied to assess the pathogenicity of the identified variant. Intracytoplasmic sperm injection (ICSI) was used to assist fertilization for the patient with teratozoospermia.Results
We performed whole-exome sequencing (WES) and detected a novel homozygous frameshift mutation of c.335_336del [p.E112Vfs*3] in DNAJB13 on a primary infertile male patient. Intrigu
SUBMITTER: Liu M
PROVIDER: S-EPMC8995218 | biostudies-literature | 2022 Mar
REPOSITORIES: biostudies-literature