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24. [A case of congenital non-spherocytic hemolytic anemia caused by triose phosphate isomerase deficiency. Prenatal diagnosis]. Poinsot J, Parent P, Alix D, Toudic L, Castel Y. J Genet Hum; 1986 Nov; 34(5):431-7. PubMed ID: 3794669 [Abstract] [Full Text] [Related]
25. Possibility of prenatal diagnosis of hereditary triose phosphate isomerase deficiency. Rosa R, Prehu MO, Calvin MC, Daffos F, Forestier F. Prenat Diagn; 1986 Nov; 6(3):231-4. PubMed ID: 3725742 [Abstract] [Full Text] [Related]
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27. Glucose Phosphate Isomerase Deficiency: High Prevalence of p.Arg347His Mutation in Indian Population Associated with Severe Hereditary Non-Spherocytic Hemolytic Anemia Coupled with Neurological Dysfunction. Kedar PS, Dongerdiye R, Chilwirwar P, Gupta V, Chiddarwar A, Devendra R, Warang P, Prasada H, Sampagar A, Bhat S, Chandrakala S, Madkaikar M. Indian J Pediatr; 2019 Aug 28; 86(8):692-699. PubMed ID: 31030358 [Abstract] [Full Text] [Related]
29. Triosephosphate isomerase deficiency: new insights into an enigmatic disease. Orosz F, Oláh J, Ovádi J. Biochim Biophys Acta; 2009 Dec 28; 1792(12):1168-74. PubMed ID: 19786097 [Abstract] [Full Text] [Related]
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