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For: Gilfix BM. Congenital disorders of glycosylation and the challenge of rare diseases. Hum Mutat 2019;40:1010-2. [PMID: 31374155 DOI: 10.1002/humu.23829] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]
Number Citing Articles
1 Totoń-Żurańska J, Kapusta P, Rybak-Krzyszkowska M, Lorenc K, Machlowska J, Skalniak A, Filipek E, Pawlik D, Wołkow PP. Contribution of a Novel B3GLCT Variant to Peters Plus Syndrome Discovered by a Combination of Next-Generation Sequencing and Automated Text Mining. Int J Mol Sci 2019;20:E6006. [PMID: 31795264 DOI: 10.3390/ijms20236006] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
2 Paprocka J, Jezela-Stanek A, Tylki-Szymańska A, Grunewald S. Congenital Disorders of Glycosylation from a Neurological Perspective. Brain Sci 2021;11:88. [PMID: 33440761 DOI: 10.3390/brainsci11010088] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]