BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: 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]
Number Citing Articles
1 Pshenichnikova OS, Goncharova MV, Pustovoit YS, Karpova IV, Surin VL. PILOT RESEARCH OF A GENETIC PREDISPOSITION FOR CLINICAL MANIFESTATIONS OF ACUTE INTERMITTENT PORPHYRIA. Gematologiâ i transfuziologiâ 2019;64:123-137. [DOI: 10.35754/0234-5730-2019-64-2-123-137] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
2 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]