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Cited by in F6Publishing
For: Alfadhel M, Umair M, Almuzzaini B, Asiri A, Al Tuwaijri A, Alhamoudi K, Alyafee Y, Al-Owain M. Identification of the TTC26 Splice Variant in a Novel Complex Ciliopathy Syndrome with Biliary, Renal, Neurological, and Skeletal Manifestations. Mol Syndromol 2021;12:133-40. [PMID: 34177428 DOI: 10.1159/000513829] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]
Number Citing Articles
1 Klaab Z, Tuwaijri AA, Umair M, Aldahmash B, Alfadhel M. A novel homozygous splice site variant in the CLCN7 causes osteopetrosis. Journal of King Saud University - Science 2023;35:102377. [DOI: 10.1016/j.jksus.2022.102377] [Reference Citation Analysis]
2 Chen W, Wang F, Zeng W, Zhang X, Shen L, Zhang Y, Zhou X. Biallelic mutations of TTC12 and TTC21B were identified in Chinese patients with multisystem ciliopathy syndromes. Hum Genomics 2022;16:48. [PMID: 36273201 DOI: 10.1186/s40246-022-00421-z] [Reference Citation Analysis]
3 Al Tuwaijri A, Alyafee Y, Alharbi M, Ballow M, Aldrees M, Alam Q, Sleiman RA, Umair M, Alfadhel M. Novel homozygous pathogenic mitochondrial DNAJC19 variant in a patient with dilated cardiomyopathy and global developmental delay. Mol Genet Genomic Med 2022;:e1969. [PMID: 35611801 DOI: 10.1002/mgg3.1969] [Reference Citation Analysis]