For citations:
Berezhanskaya S.B., Afonin A.A., Vostrikh N.N., Lazareva K.I., Loginova I.G., Kravchenko L.V., Medoyan A.V., Monat L.I. 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. Medical Herald of the South of Russia. 2023;14(1):56-65. (In Russ.) https://doi.org/10.21886/2219-8075-2023-14-1-56-65
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