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Original Articles

Hemolytic Anemia and Metabolic Acidosis: Think about Glutathione Synthetase Deficiency

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Pages 18-20 | Received 11 Feb 2014, Accepted 14 Jul 2014, Published online: 28 Aug 2014

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Ipek Guney Varal, Pelin Dogan, Orhan Gorukmez, Sevil Dorum & Arzu Akdag. (2020) Glutathione synthetase deficiency: a novel mutation with femur agenesis. Fetal and Pediatric Pathology 39:1, pages 38-44.
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Articles from other publishers (4)

Xiaohang Chen, Hongyan Chen, Haimei Nie, Gaochi Li, Jinjiang Su, Xianzhen Cao, Yongli Cao & Fengxiang Wei. (2021) Amniotic fluid metabolomic and lipidomic alterations associated with hemoglobin Bart’s diseases. Metabolomics 17:9.
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H. Xia, J. Ye, L. Wang, J. Zhu & Z. He. (2018) A case of severe glutathione synthetase deficiency with novel GSS mutations. Brazilian Journal of Medical and Biological Research 51:3.
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Paldeep S Atwal, Casey R Medina, Lindsay C Burrage & V Reid Sutton. (2016) Nineteen-year follow-up of a patient with severe glutathione synthetase deficiency. Journal of Human Genetics 61:7, pages 669-672.
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Mehmet Gündüz, Özlem Ünal, Sumru Kavurt, Emrecan Türk & Neslihan Önenli Mungan. (2016) Clinical findings and effect of sodium hydrogen carbonate in patients with glutathione synthetase deficiency. Journal of Pediatric Endocrinology and Metabolism 29:4.
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