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    A clinical case of a familial form of hereditary metabolic disease from the group of peroxisomal diseases (D-bifunctional protein deficiency) in the neonatal period

    A clinical case of a familial form of hereditary metabolic disease from the group of peroxisomal diseases (D-bifunctional protein deficiency) in the neonatal period by S. B. Berezhanskaya, A. A. Afonin, N. N. Vostrikh, K. I. Lazareva, I. G. Loginova, L. V. Kravchenko, A. V. Medoyan, L. I. Monat

    Published 2023-03-01
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