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Cited by in F6Publishing
For: Adutwum M, Hurst A, Mirzaa G, Kushner JD, Rogers C, Khalek N, Cristancho AG, Burrill N, Seifert ME, Scarano MI, Schnur RE, Slavotinek A. Six new cases of CRB2-related syndrome and a review of clinical findings in 28 reported patients. Clin Genet 2023;103:97-102. [PMID: 36071576 DOI: 10.1111/cge.14222] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Tessier A, Roux N, Boutaud L, Lunel E, Hakkakian L, Parisot M, Garfa-Traoré M, Ichkou A, Elkhartoufi N, Bole C, Nitschke P, Amiel J, Martinovic J, Encha-Razavi F, Attié-Bitach T, Thomas S. Bi-allelic variations in CRB2, encoding the crumbs cell polarity complex component 2, lead to non-communicating hydrocephalus due to atresia of the aqueduct of sylvius and central canal of the medulla. Acta Neuropathol Commun 2023;11:29. [PMID: 36803301 DOI: 10.1186/s40478-023-01519-8] [Reference Citation Analysis]
2 Simaab A, Krishin J, Alaradi SR, Haider N, Shah M, Ullah A, Abdullah A, Ahmad W, Hansen T, Basit S. Exome Sequencing Revealed a Novel Splice Site Variant in the CRB2 Gene Underlying Nephrotic Syndrome. Medicina (Kaunas) 2022;58. [PMID: 36556986 DOI: 10.3390/medicina58121784] [Reference Citation Analysis]