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

doi:10.12998/wjcc.v10.i34.12761

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Dec 6, 2022 (publication date) through Dec 25, 2024

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World Journal of Clinical Cases

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2307-8960

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Clin Cases. Dec 6, 2022; 10(34): 12761-12767
Published online Dec 6, 2022. doi: 10.12998/wjcc.v10.i34.12761

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Figure 1 Eosin staining (Y-E): Arrows, tailless sperm heads; triangles, headless sperm tails.

Citation: 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
URL: https://www.wjgnet.com/2307-8960/full/v10/i34/12761.htm
DOI: https://dx.doi.org/10.12998/wjcc.v10.i34.12761