Triosephosphate isomerase deficiency (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Triosephosphate isomerase deficiency" in English language version.

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Ralser, Markus; Gino Heeren; Michael Breitenbach; Hans Lehrach; Sylvia Krobitsch (December 20, 2006). Janbon, Guilhem (ed.). "Triose Phosphate Isomerase Deficiency Is Caused by Altered Dimerization–Not Catalytic Inactivity–of the Mutant Enzymes". PLOS ONE. 1 (1): e30. Bibcode:2006PLoSO...1...30R. doi:10.1371/journal.pone.0000030. PMC 1762313. PMID 17183658.
Schneider, Arthur S.; William N. Valentine; Hattori M; H. L. Heins Jr (1965). "Hereditary Hemolytic Anemia with Triosephosphate Isomerase Deficiency". New England Journal of Medicine. 272 (5): 229–235. doi:10.1056/NEJM196502042720503. PMID 14242501.
Schneider, Arthur S. (Mar 2000). "Triosephosphate isomerase deficiency: historical perspectives and molecular aspects". Best Practice & Research Clinical Haematology. 13 (1): 119–140. doi:10.1053/beha.2000.0061. PMID 10916682.
Schneider A, Westwood B, Yim C, et al. (1996). "The 1591C mutation in triosephosphate isomerase (TPI) deficiency. Tightly linked polymorphisms and a common haplotype in all known families". Blood Cells Mol. Dis. 22 (2): 115–25. doi:10.1006/bcmd.1996.0019. PMID 8931952.

Ralser, Markus; Gino Heeren; Michael Breitenbach; Hans Lehrach; Sylvia Krobitsch (December 20, 2006). Janbon, Guilhem (ed.). "Triose Phosphate Isomerase Deficiency Is Caused by Altered Dimerization–Not Catalytic Inactivity–of the Mutant Enzymes". PLOS ONE. 1 (1): e30. Bibcode:2006PLoSO...1...30R. doi:10.1371/journal.pone.0000030. PMC 1762313. PMID 17183658.
Schneider, Arthur S.; William N. Valentine; Hattori M; H. L. Heins Jr (1965). "Hereditary Hemolytic Anemia with Triosephosphate Isomerase Deficiency". New England Journal of Medicine. 272 (5): 229–235. doi:10.1056/NEJM196502042720503. PMID 14242501.
Schneider, Arthur S. (Mar 2000). "Triosephosphate isomerase deficiency: historical perspectives and molecular aspects". Best Practice & Research Clinical Haematology. 13 (1): 119–140. doi:10.1053/beha.2000.0061. PMID 10916682.
Schneider A, Westwood B, Yim C, et al. (1996). "The 1591C mutation in triosephosphate isomerase (TPI) deficiency. Tightly linked polymorphisms and a common haplotype in all known families". Blood Cells Mol. Dis. 22 (2): 115–25. doi:10.1006/bcmd.1996.0019. PMID 8931952.