BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Schneider-yin X, Hergersberg M, Schuurmans MM, Gregor A, Minder EI. Mutation hotspots in the human porphobilinogen deaminase gene: Recurrent mutations G111R and R173Q occurring at CpG motifs. J Inherit Metab Dis 2004;27:625-31. [DOI: 10.1023/b:boli.0000042936.20691.ad] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 0.4] [Reference Citation Analysis]
Number Citing Articles
1 Sirch C, Khanna N, Frassetto L, Bianco F, Artero ML. Diagnosis of acute intermittent porphyria in a renal transplant patient: A case report. World J Transplant 2022; 12(1): 8-14 [DOI: 10.5500/wjt.v12.i1.8] [Reference Citation Analysis]
2 Tortorelli S, White AL, Raymond K. Disorders of porphyrin metabolism. Biochemical and Molecular Basis of Pediatric Disease 2021. [DOI: 10.1016/b978-0-12-817962-8.00031-7] [Reference Citation Analysis]
3 Yuan T, Li YH, Wang X, Gong FY, Wu XY, Fu Y, Zhao WG. Acute Intermittent Porphyria: A Diagnostic Challenge for Endocrinologist. Chin Med J (Engl). 2015;128:1980-1981. [PMID: 26168842 DOI: 10.4103/0366-6999.160621] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 0.7] [Reference Citation Analysis]
4 Schneider-Yin X, van Tuyll van Serooskerken AM, Siegesmund M, Went P, Barman-Aksözen J, Bladergroen RS, Komminoth P, Cloots RH, Winnepenninckx VJ, zur Hausen A, Weber M, Driessen A, Poblete-Gutiérrez P, Bauer P, Schroeder C, van Geel M, Minder EI, Frank J. Biallelic inactivation of protoporphyrinogen oxidase and hydroxymethylbilane synthase is associated with liver cancer in acute porphyrias. J Hepatol 2015;62:734-8. [PMID: 25445397 DOI: 10.1016/j.jhep.2014.11.029] [Cited by in Crossref: 19] [Cited by in F6Publishing: 18] [Article Influence: 2.4] [Reference Citation Analysis]
5 Susa S, Daimon M, Kato T, Maeda N. A novel G168X mutation and a recurrent 730-731delCT mutation of the porphobilinogen deaminase gene in Japanese patients with acute intermittent porphyria. Blood Cells Mol Dis 2013;51:130-1. [PMID: 23582379 DOI: 10.1016/j.bcmd.2013.02.008] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]
6 Surin VL, Luchinina YA, Selivanova DS, Pustovoit YS, Karpova IV, Pivnik AV, Luk’ianenko AV, Kravchenko SK. Molecular genetic study of acute intermittent porphyria in Russia: Mutation analysis and functional polymorphism search in porphobilinogen deaminase gene. Russ J Genet 2010;46:476-87. [DOI: 10.1134/s1022795410040149] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]