BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Schmidt L, Wain KE, Hajek C, Estrada-Veras JI, Guillen Sacoto MJ, Wentzensen IM, Malhotra A, Clause A, Perry D, Moreno-De-Luca A, Bell M. Expanding the Phenotype of TUBB2A-Related Tubulinopathy: Three Cases of a Novel, Heterozygous TUBB2A Pathogenic Variant p.Gly98Arg. Mol Syndromol 2021;12:33-40. [PMID: 33776625 DOI: 10.1159/000512160] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Clark LN, Gao Y, Wang GT, Hernandez N, Ashley-koch A, Jankovic J, Ottman R, Leal SM, Rodriguez SMB, Louis ED. Whole genome sequencing identifies candidate genes for familial essential tremor and reveals biological pathways implicated in essential tremor aetiology. eBioMedicine 2022;85:104290. [DOI: 10.1016/j.ebiom.2022.104290] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
2 Pan X, Liu S, Liu L, Zhang X, Yao H, Tan B. Case Report: Exome and RNA Sequencing Identify a Novel de novo Missense Variant in HNRNPK in a Chinese Patient With Au-Kline Syndrome. Front Genet 2022;13:853028. [PMID: 35422839 DOI: 10.3389/fgene.2022.853028] [Reference Citation Analysis]