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Cited by in F6Publishing
For: Song D, Dai Y, Chen X, Fu X, Chang X, Wang N, Zhang C, Yan C, Zheng H, Wu L, Jiang L, Hua Y, Yang H, Wang Z, Dai T, Zhu W, Han C, Yuan Y, Kobayashi K, Toda T, Xiong H. Genetic variations and clinical spectrum of dystroglycanopathy in a large cohort of Chinese patients. Clin Genet 2021;99:384-95. [PMID: 33200426 DOI: 10.1111/cge.13886] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
Number Citing Articles
1 Zago S, Silvestri E, Arcangeli T, Calisesi M, Romeo C, Parmeggiani G, Parrini E, Cetica V, Guerrini R, Palicelli A, Bonasoni MP. Fetal Presentation of Walker-Warburg Syndrome with Compound Heterozygous POMT2 Missense Mutations. Fetal Pediatr Pathol 2022;:1-8. [PMID: 36048137 DOI: 10.1080/15513815.2022.2116620] [Reference Citation Analysis]
2 Yang H, Song D, Liu Y, Chen X, Zhu Y, Wei C, Fu X, Liu X, Yang Z, Xiong H. Seizures and EEG characteristics in a cohort of pediatric patients with dystroglycanopathies. Seizure 2022;101:39-47. [PMID: 35863218 DOI: 10.1016/j.seizure.2022.07.008] [Reference Citation Analysis]
3 Lallar M, Kaur L, Preet M, Singh UP. B4GAT1 Gene Associated Congenital Muscular Dystrophy Presenting with Recurrent Severe Ventriculomegaly: Case Report and Review of Literature. Fetal Pediatr Pathol 2021;:1-6. [PMID: 34587870 DOI: 10.1080/15513815.2021.1982091] [Reference Citation Analysis]
4 Zambon AA, Muntoni F. Congenital muscular dystrophies: What is new? Neuromuscul Disord 2021;31:931-42. [PMID: 34470717 DOI: 10.1016/j.nmd.2021.07.009] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 5.0] [Reference Citation Analysis]
5 Chen XY, Song DY, Jiang L, Tan DD, Liu YD, Liu JY, Chang XZ, Xing GG, Toda T, Xiong H. Phenotype and Genotype Study of Chinese POMT2-Related α-Dystroglycanopathy. Front Genet 2021;12:692479. [PMID: 34413876 DOI: 10.3389/fgene.2021.692479] [Reference Citation Analysis]