For citations:
Dmitriev A.V., Fedina N.V., Gudkov R.A., Petrova V.I., Bozhenova L.V. A clinical case of galactosemia type I in a child with a compound heterozygous mutation in the gene: C.267CG (p. Tyr89Term), C.563A (p.Gln188Arg). Medical alphabet. 2025;(6):22-25. (In Russ.) https://doi.org/10.33667/2078-5631-2025-6-22-25
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