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Year | Number of Results |
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2013 | 1 |
2014 | 1 |
2019 | 1 |
2020 | 1 |
2024 | 0 |
PubMed (GeneRIF) for id: 3321
3 results
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IGSF3 mutation identified in patient with severe COPD alters cell function and motility.
JCI Insight. 2020 Jul 23;5(14):e138101. doi: 10.1172/jci.insight.138101.
JCI Insight. 2020.
PMID: 32573489
Free PMC article.
Osteoclastogenesis inhibition by mutated IGSF23 results in human osteopetrosis.
Yuan Y, Yang L, Liu T, Zhang H, Lu Q.
Yuan Y, et al.
Cell Prolif. 2019 Nov;52(6):e12693. doi: 10.1111/cpr.12693. Epub 2019 Sep 27.
Cell Prolif. 2019.
PMID: 31560140
Free PMC article.
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Identification of an IGSF3 mutation in a family with congenital nasolacrimal duct obstruction.
Foster J 2nd, Kapoor S, Diaz-Horta O, Singh A, Abad C, Rastogi A, Moharana R, Tekeli O, Walz K, Tekin M.
Foster J 2nd, et al.
Clin Genet. 2014 Dec;86(6):589-91. doi: 10.1111/cge.12321. Epub 2013 Dec 27.
Clin Genet. 2014.
PMID: 24372406
No abstract available.
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