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pro vyhledávání: '"Nawarah Alhamoud"'
Publikováno v:
Heart Views, Vol 25, Iss 1, Pp 35-36 (2024)
3-Methylcrotonyl-CoA carboxylase (3-MCC) deficiency is a rare autosomal recessive disease of leucine catabolism. 3-MCC deficiency may lead to metabolic decompensation under stress; however, outcomes of elective surgery requiring cardiopulmonary bypas
Externí odkaz:
https://doaj.org/article/0890f489e6e44119aab17aa1265341a2
