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Deng TQ, Xie YL, Pu JB, Xuan J, Li XM. Compound heterozygous mutations in PMFBP1 cause acephalic spermatozoa syndrome: A case report. World J Clin Cases 2022; 10(34): 12761-12767 [PMID: 36579083 DOI: 10.12998/wjcc.v10.i34.12761]
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