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Tam CS, Kantarjian H, Garcia-Manero G, Borthakur G , O'Brien S, Ravandi F, Shan J, Cortes J

L-2-HGA is an autosomal recessive encephalopathy with an onset in childhood that causes developmental delays, epilepsy and cerebellar ataxia, the traditional clinical signs of this condition

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Abstract Lack of effective drugs for acute kidney injury (AKI) grades 12 is a crucial challenge in clinic

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