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Cited by in F6Publishing
For: Xia H, Huang X, Deng S, Xu H, Yang Y, Liu X, Yuan L, Deng H. DNAH11 compound heterozygous variants cause heterotaxy and congenital heart disease. PLoS One 2021;16:e0252786. [PMID: 34133440 DOI: 10.1371/journal.pone.0252786] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Dong S, Bei F, Yu T, Sun L, Chen X, Yan H. A Novel Compound Heterozygous Mutation in the DNAH11 Gene Found in Neonatal Twins With Primary Ciliary Dyskinesis. Front Genet 2022;13:814511. [PMID: 35295944 DOI: 10.3389/fgene.2022.814511] [Reference Citation Analysis]
2 Demir Eksi D, Yilmaz E, Basaran AE, Erduran G, Nur B, Mihci E, Karadag B, Bingol A, Alper OM. Novel Gene Variants Associated with Primary Ciliary Dyskinesia. Indian J Pediatr 2022. [PMID: 35239159 DOI: 10.1007/s12098-022-04098-z] [Reference Citation Analysis]