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Cited by in F6Publishing
For: Majore S, Agolini E, Micale L, Pascolini G, Zuppi P, Cocciadiferro D, Morlino S, Mattiuzzo M, Valiante M, Castori M, Novelli A, Grammatico P. Clinical presentation and molecular characterization of a novel patient with variant POC1A-related syndrome. Clin Genet 2021;99:540-6. [PMID: 33372278 DOI: 10.1111/cge.13911] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Li G, Chang G, Wang C, Yu T, Li N, Huang X, Wang X, Wang J, Wang J, Yao R. Identification of SOFT syndrome caused by a pathogenic homozygous splicing variant of POC1A: a case report. BMC Med Genomics 2021;14:207. [PMID: 34419044 DOI: 10.1186/s12920-021-01055-1] [Reference Citation Analysis]
2 Batu Oto B, Ağırbaşlı D, Kılıçarslan O, Celik G, Kalayci Yigin A, Seven M, Yetik H. Pigmentary retinopathy with perivascular sparing in a SOFT syndrome patient with a novel homozygous splicing variant in POC1A gene. Ophthalmic Genet 2022;:1-4. [PMID: 35930384 DOI: 10.1080/13816810.2022.2103837] [Reference Citation Analysis]
3 Zhao Q, Gao S, Chen X, Zhu X. POC1A, prognostic biomarker of immunosuppressive microenvironment in cancer. Aging (Albany NY) 2022;14. [PMID: 35748773 DOI: 10.18632/aging.204141] [Reference Citation Analysis]