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Cited by in F6Publishing
For: Anttonen A, Lehesjoki A. Reply: The phenotypic and molecular spectrum of PEHO syndrome and PEHO-like disorders. Brain 2017;140:e50-e50. [DOI: 10.1093/brain/awx157] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.4] [Reference Citation Analysis]
Number Citing Articles
1 Sabaie H, Ahangar NK, Ghafouri-Fard S, Taheri M, Rezazadeh M. Clinical and genetic features of PEHO and PEHO-Like syndromes: A scoping review. Biomed Pharmacother 2020;131:110793. [PMID: 33152950 DOI: 10.1016/j.biopha.2020.110793] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
2 Õunap K, Muru K, Õiglane-Shlik E, Ilves P, Pajusalu S, Kuus I, Wojcik MH, Reimand T. PEHO syndrome caused by compound heterozygote variants in ZNHIT3 gene. Eur J Med Genet 2020;63:103660. [PMID: 31048081 DOI: 10.1016/j.ejmg.2019.04.017] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.3] [Reference Citation Analysis]