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pro vyhledávání: '"Karina Paula Borges"'
Autor:
Carla Diniz Dias Fernandes, Yasmin Lima Witzel, Laryssa Gomes Heredia, Carolina Toledo Scarpa, Karina Paula Borges, Rosa Cristina Coutinho
Publikováno v:
Residência Pediátrica, Vol 14, Iss 1 (2024)
Propionic acidemia is part of the organic acidemias that constitute a group of inherited autosomal recessive diseases caused by the deficiency of enzymes involved in the catabolism of branched-chain amino acids resulting in the tissue accumulation of
Externí odkaz:
https://doaj.org/article/c14c02c62da9416d8c177aaac6e4a68f