For citations:
Momot G.O., Shalygina A.A., Krukovich E.V., Zelenkova I.S. Menkes disease. A clinical case of a rare disorder of copper metabolism caused by a mutation in the ATP7A gene. Yakut Medical Journal. 2021;(3):116-118. https://doi.org/10.25789/YMJ.2021.75.30
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