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For: Tvina A, Thomsen A, Palatnik A. Prenatal and postnatal phenotype of a pathologic variant in the ATP6AP1 gene. Eur J Med Genet 2020;63:103881. [PMID: 32058063 DOI: 10.1016/j.ejmg.2020.103881] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Yang X, Lv Z, Tang Q, Chen X, Huang L, Yang M, Lan L, Shan Q. Congenital disorder of glycosylation caused by mutation of ATP6AP1 gene (c.1036G>A) in a Chinese infant: A case report. WJCC 2021;9:7876-85. [DOI: 10.12998/wjcc.v9.i26.7876] [Reference Citation Analysis]
2 Bogdańska A, Lipiński P, Szymańska-Rożek P, Jezela-Stanek A, Rokicki D, Socha P, Tylki-Szymańska A. Clinical, biochemical and molecular phenotype of congenital disorders of glycosylation: long-term follow-up. Orphanet J Rare Dis 2021;16:17. [PMID: 33407696 DOI: 10.1186/s13023-020-01657-5] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 4.0] [Reference Citation Analysis]
3 Komlosi K, Gläser S, Kopp J, Hotz A, Alter S, Zimmer AD, Beger C, Heinzel S, Schmidt C, Fischer J. Neonatal presentation of COG6-CDG with prominent skin phenotype. JIMD Rep 2020;55:51-8. [PMID: 32905044 DOI: 10.1002/jmd2.12154] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]