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Cited by in F6Publishing
For: Conte F, Morava E, Bakar NA, Wortmann SB, Poerink AJ, Grunewald S, Crushell E, Al-Gazali L, de Vries MC, Mørkrid L, Hertecant J, Brocke Holmefjord KS, Kronn D, Feigenbaum A, Fingerhut R, Wong SY, van Scherpenzeel M, Voermans NC, Lefeber DJ. Phosphoglucomutase-1 deficiency: Early presentation, metabolic management and detection in neonatal blood spots. Mol Genet Metab 2020;131:135-46. [PMID: 33342467 DOI: 10.1016/j.ymgme.2020.08.003] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Conte F, van Buuringen N, Voermans NC, Lefeber DJ. Galactose in human metabolism, glycosylation and congenital metabolic diseases: Time for a closer look. Biochim Biophys Acta Gen Subj 2021;1865:129898. [PMID: 33878388 DOI: 10.1016/j.bbagen.2021.129898] [Reference Citation Analysis]
2 Pi S, Gong J, Xiao W, Xiao B, Mao X, Long H. The second DDOST-CDG patient with lactose intolerance, developmental delay, and situs inversus totalis. J Hum Genet 2021. [PMID: 34462534 DOI: 10.1038/s10038-021-00974-2] [Reference Citation Analysis]
3 Park JH, Marquardt T. Treatment Options in Congenital Disorders of Glycosylation. Front Genet 2021;12:735348. [PMID: 34567084 DOI: 10.3389/fgene.2021.735348] [Reference Citation Analysis]