← Evidence map

ArticleWorld journal of clinical cases2022

Compound heterozygous mutations in PMFBP1 cause acephalic spermatozoa syndrome: A case report.

Tian-Qin Deng et al.PubMed ↗Full text ↗Publisher ↗

No numbers read from the abstract.

6 papers cite it

2022
2023
2024
2025
2026
this papercites it
Full record →Abstract, authors, funding and every citing paper · PMID 36579083