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Cited by in F6Publishing
For: Feng J, Lan X, Shen J, Song X, Tang X, Xu W, Ren X, Zhang H, Yu G, Wu S. A de novo MAPRE2 variant in a patient with congenital symmetric circumferential skin creases type 2. Mol Genet Genomic Med 2020;8:e1096. [PMID: 31903734 DOI: 10.1002/mgg3.1096] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
Number Citing Articles
1 Jiang B, Xiao F, Li X, Xiao Y, Wang Y, Zhang T. Case Report: Pediatric Recurrent Acute Liver Failure Caused by Neuroblastoma Amplified Sequence (NBAS) Gene Mutations. Front Pediatr 2020;8:607005. [PMID: 33520894 DOI: 10.3389/fped.2020.607005] [Reference Citation Analysis]
2 Feng J, Lan X, Shen J, Song X, Tang X, Xu W, Ren X, Zhang H, Yu G, Wu S. A de novo MAPRE2 variant in a patient with congenital symmetric circumferential skin creases type 2. Mol Genet Genomic Med 2020;8:e1096. [PMID: 31903734 DOI: 10.1002/mgg3.1096] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
3 Chun Fang G, Kaiwei D, Lingkong Z, Xuwei T. Diaphragmatic paralysis in a neonate with circumferential skin creases Kunze type. Mol Genet Genomic Med 2022;:e2003. [PMID: 35747986 DOI: 10.1002/mgg3.2003] [Reference Citation Analysis]
4 Chaudhuri T, Chintalapati J, Hosur MV. Identification of 3'-UTR single nucleotide variants and prediction of select protein imbalance in mesial temporal lobe epilepsy patients. PLoS One 2021;16:e0252475. [PMID: 34086756 DOI: 10.1371/journal.pone.0252475] [Reference Citation Analysis]
5 Tang X, Lan X, Song X, Xu W, Zhang Y, Zhang H, Wu S. De novo variants in WDR45 underlie beta-propeller protein-associated neurodegeneration in five independent families. Mol Genet Genomic Med 2020;8:e1499. [PMID: 33037762 DOI: 10.1002/mgg3.1499] [Cited by in F6Publishing: 1] [Reference Citation Analysis]