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Clinical findings of patients with hyperammonemia affected by urea cycle disorders with hepatic encephalopathy.
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- International Journal of Developmental Neuroscience, 2022, v. 82, n. 8, p. 772, doi. 10.1002/jdn.10229
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Clinical, biochemical and molecular findings of 24 Brazilian patients with glutaric acidemia type 1: 4 novel mutations in the GCDH gene.
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- Metabolic Brain Disease, 2021, v. 36, n. 2, p. 205, doi. 10.1007/s11011-020-00632-0
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- Article