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Cited by in F6Publishing
For: Chen Q, Bao H, Wu H, Zhao S, Huang S, Zhao F. Diagnosis of cobalamin C deficiency with renal abnormality from onset in a Chinese child by next generation sequencing: A case report. Exp Ther Med 2017;14:3637-43. [PMID: 29042959 DOI: 10.3892/etm.2017.4970] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 0.8] [Reference Citation Analysis]
Number Citing Articles
1 Yang J, Wang L, Huang Y, Liu K, Lu C, Si N, Wang R, Liu Y, Zhang X. Keratin 5-Cre-driven deletion of Ncstn in an acne inversa-like mouse model leads to a markedly increased IL-36a and Sprr2 expression. Front Med 2020;14:305-17. [DOI: 10.1007/s11684-019-0722-8] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
2 Xu J, Zhang A, Huang F. Biallelic mutations in carbamoyl phosphate synthetase 1 induced hyperammonemia in a neonate: A case report. Exp Ther Med 2020;20:623-9. [PMID: 32537019 DOI: 10.3892/etm.2020.8717] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
3 Zhang W, Yang Y, Peng W, Chang J, Mei Y, Yan L, Chen Y, Wei X, Liu Y, Wang Y, Feng Z. A 7-Year Report of Spectrum of Inborn Errors of Metabolism on Full-Term and Premature Infants in a Chinese Neonatal Intensive Care Unit. Front Genet 2019;10:1302. [PMID: 31998365 DOI: 10.3389/fgene.2019.01302] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
4 Smith HS, Swint JM, Lalani SR, Yamal JM, de Oliveira Otto MC, Castellanos S, Taylor A, Lee BH, Russell HV. Clinical Application of Genome and Exome Sequencing as a Diagnostic Tool for Pediatric Patients: a Scoping Review of the Literature. Genet Med 2019;21:3-16. [PMID: 29760485 DOI: 10.1038/s41436-018-0024-6] [Cited by in Crossref: 41] [Cited by in F6Publishing: 38] [Article Influence: 10.3] [Reference Citation Analysis]
5 Wang Q, Wang Q, Gao Y, Tang C, Gao Z, Hu Z. Case Report: Membranous Nephropathy Secondary to Cobalamin C Disease. Front Med 2022;8:807017. [DOI: 10.3389/fmed.2021.807017] [Reference Citation Analysis]