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Cited by in F6Publishing
For: Zhang P, Wu B, Lu Y, Ni Q, Liu R, Zhou W, Wang H. First maternal uniparental disomy for chromosome 2 with PREPL novel frameshift mutation of congenital myasthenic syndrome 22 in an infant. Mol Genet Genomic Med 2020;8:e1144. [PMID: 31985178 DOI: 10.1002/mgg3.1144] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Qian Y, Wu B, Liu R, Lu Y, Zhang P, Shao C, Huang Y, Wang H. Case Report: Complete Maternal Uniparental Isodisomy of Chromosome 5 (iUPD(5)mat) With PCSK1 Nonsense Variant in an Infant With Recurrent Diarrhea. Front Genet 2021;12:668326. [PMID: 34025722 DOI: 10.3389/fgene.2021.668326] [Reference Citation Analysis]
2 Shchagina O, Bessonova L, Bychkov I, Beskorovainaya T, Poliakov A. A Family Case of Congenital Myasthenic Syndrome-22 Induced by Different Combinations of Molecular Causes in Siblings. Genes (Basel) 2020;11:E821. [PMID: 32707643 DOI: 10.3390/genes11070821] [Reference Citation Analysis]
3 Zhang P, Wu B, Lu Y, Ni Q, Liu R, Zhou W, Wang H. First maternal uniparental disomy for chromosome 2 with PREPL novel frameshift mutation of congenital myasthenic syndrome 22 in an infant. Mol Genet Genomic Med 2020;8:e1144. [PMID: 31985178 DOI: 10.1002/mgg3.1144] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]