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Year | Number of Results |
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2016 | 1 |
2020 | 2 |
2021 | 1 |
2024 | 0 |
PubMed (GeneRIF) for id: 159686
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Biallelic mutations of CFAP58 are associated with multiple morphological abnormalities of the sperm flagella.
Clin Genet. 2021 Mar;99(3):443-448. doi: 10.1111/cge.13898. Epub 2020 Dec 18.
Clin Genet. 2021.
PMID: 33314088
Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice.
He X, Liu C, Yang X, Lv M, Ni X, Li Q, Cheng H, Liu W, Tian S, Wu H, Gao Y, Yang C, Tan Q, Cong J, Tang D, Zhang J, Song B, Zhong Y, Li H, Zhi W, Mao X, Fu F, Ge L, Shen Q, Zhang M, Saiyin H, Jin L, Xu Y, Zhou P, Wei Z, Zhang F, Cao Y.
He X, et al.
Am J Hum Genet. 2020 Sep 3;107(3):514-526. doi: 10.1016/j.ajhg.2020.07.010. Epub 2020 Aug 12.
Am J Hum Genet. 2020.
PMID: 32791035
Free PMC article.
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Focused Analysis of Exome Sequencing Data for Rare Germline Mutations in Familial and Sporadic Lung Cancer.
Liu Y, Kheradmand F, Davis CF, Scheurer ME, Wheeler D, Tsavachidis S, Armstrong G, Simpson C, Mandal D, Kupert E, Anderson M, You M, Xiong D, Pikielny C, Schwartz AG, Bailey-Wilson J, Gaba C, De Andrade M, Yang P, Pinney SM; Genetic Epidemiology of Lung Cancer Consortium; Amos CI, Spitz MR.
Liu Y, et al.
J Thorac Oncol. 2016 Jan;11(1):52-61. doi: 10.1016/j.jtho.2015.09.015.
J Thorac Oncol. 2016.
PMID: 26762739
Free PMC article.
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