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Autor:
Olga V. Bugun, Galina P. Bogonosova, Tatyana A. Astakhova, Tatyana A. Bairova, Natalya N. Martynovich, Darya M. Barycova, Tatyana Y. Belkova, Yuliya S. Livadarova, Nanalya I. Sysoeva
Publikováno v:
Вопросы современной педиатрии, Vol 23, Iss 2, Pp 96-103 (2024)
Background. Methylmalonic aciduria (MMA) is a rare disease from the group of hereditary metabolic diseases. The MMA clinical picture is polymorphic and meanwhile similar to other metabolic disorders. Determination of specific metabolites in biologica
Externí odkaz:
https://doaj.org/article/1d308db1c8e041368ebb1b2c6d76fb2b
