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Year | Number of Results |
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2021 | 1 |
2022 | 1 |
2023 | 2 |
2024 | 1 |
PubMed (GeneRIF) for id: 286464
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Mutations in CFAP47, a previously reported MMAF causative gene, also contribute to the respiratory defects in patients with PCD.
Mol Genet Genomic Med. 2024 Jan;12(1):e2278. doi: 10.1002/mgg3.2278. Epub 2023 Sep 18.
Mol Genet Genomic Med. 2024.
PMID: 37723893
Free PMC article.
A novel mutation in CFAP47 causes male infertility due to multiple morphological abnormalities of the sperm flagella.
Liu M, Dai S, Zhang J, Yang Y, Shen Y, Liu H, Yang Y, Jiang C, Tian E.
Liu M, et al.
Front Endocrinol (Lausanne). 2023 Jun 23;14:1155639. doi: 10.3389/fendo.2023.1155639. eCollection 2023.
Front Endocrinol (Lausanne). 2023.
PMID: 37424856
Free PMC article.
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WDR87 interacts with CFAP47 protein in the middle piece of spermatozoa flagella to participate in sperm tail assembly.
Liao HQ, Guo ZY, Huang LH, Liu G, Lu JF, Zhang YF, Xing XW.
Liao HQ, et al.
Mol Hum Reprod. 2022 Dec 28;29(1):gaac042. doi: 10.1093/molehr/gaac042.
Mol Hum Reprod. 2022.
PMID: 36571501
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Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility.
Liu C, Tu C, Wang L, Wu H, Houston BJ, Mastrorosa FK, Zhang W, Shen Y, Wang J, Tian S, Meng L, Cong J, Yang S, Jiang Y, Tang S, Zeng Y, Lv M, Lin G, Li J, Saiyin H, He X, Jin L, Touré A, Ray PF, Veltman JA, Shi Q, O'Bryan MK, Cao Y, Tan YQ, Zhang F.
Liu C, et al.
Am J Hum Genet. 2021 Feb 4;108(2):309-323. doi: 10.1016/j.ajhg.2021.01.002. Epub 2021 Jan 19.
Am J Hum Genet. 2021.
PMID: 33472045
Free PMC article.
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