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For: Dentici M, Terracciano A, Bellacchio E, Capolino R, Novelli A, Digilio M, Dallapiccola B. Intrafamiliar clinical variability of circumferential skin creases Kunze type caused by a novel heterozygous mutation of N-terminal TUBB gene. Clinical Genetics 2018;93:1223-8. [DOI: 10.1111/cge.13232] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
Number Citing Articles
1 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]
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 Hayashi M, Wataya-Kaneda M, Koguchi-Yoshioka H, Arase N, Kubo T, Nakano H, Fujimoto M. Familial Michelin tire baby syndrome. J Dermatol 2022. [PMID: 35277884 DOI: 10.1111/1346-8138.16346] [Reference Citation Analysis]
4 Sferra A, Petrini S, Bellacchio E, Nicita F, Scibelli F, Dentici ML, Alfieri P, Cestra G, Bertini ES, Zanni G. TUBB Variants Underlying Different Phenotypes Result in Altered Vesicle Trafficking and Microtubule Dynamics. Int J Mol Sci 2020;21:E1385. [PMID: 32085672 DOI: 10.3390/ijms21041385] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 2.5] [Reference Citation Analysis]
5 Sferra A, Nicita F, Bertini E. Microtubule Dysfunction: A Common Feature of Neurodegenerative Diseases. Int J Mol Sci 2020;21:E7354. [PMID: 33027950 DOI: 10.3390/ijms21197354] [Cited by in Crossref: 9] [Cited by in F6Publishing: 9] [Article Influence: 4.5] [Reference Citation Analysis]
6 Watanabe K, Nakashima M, Kumada S, Mashimo H, Enokizono M, Yamada K, Kato M, Saitsu H. Identification of two novel de novo TUBB variants in cases with brain malformations: case reports and literature review. J Hum Genet 2021. [PMID: 34211110 DOI: 10.1038/s10038-021-00956-4] [Reference Citation Analysis]