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Cited by in F6Publishing

For:	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]

For:

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]

Number	Citing Articles
1	Gonzaga AD, de Amorim LM, Fonseca AB, Nogueira TL, Pereira OM, Nagai MA, de Oliveira Barretto OC, Ribeiro GS. Hydroxymethylbilane synthase gene mutations and polymorphisms in Brazilian families with acute intermittent porphyria. Ann Hum Genet 2015;79:162-72. [PMID: 25703257 DOI: 10.1111/ahg.12102] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]

Number

Citing Articles

Gonzaga AD, de Amorim LM, Fonseca AB, Nogueira TL, Pereira OM, Nagai MA, de Oliveira Barretto OC, Ribeiro GS. Hydroxymethylbilane synthase gene mutations and polymorphisms in Brazilian families with acute intermittent porphyria. Ann Hum Genet 2015;79:162-72. [PMID: 25703257 DOI: 10.1111/ahg.12102] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.1] [Reference Citation Analysis]