Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Antonio Anania"'
Autor:
Loredana De Pasquale, Petronilla Meo, Francesco Fulia, Antonio Anania, Valerio Meli, Antonina Mondello, Maria Tindara Raimondo, Viviana Tulino, Maria Sole Coletta, Caterina Cacace
Publikováno v:
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-5 (2022)
Abstract Background Multiple acyl-CoA dehydrogenase deficiency (MADD) or glutaric aciduria type II is an extremely rare autosomal recessive inborn error of fatty acid beta oxidation and branched-chain amino acids, secondary to mutations in the genes
Externí odkaz:
https://doaj.org/article/575fe689f38148ab89e6220f8377d4b6
Autor:
Loredana, De Pasquale, Petronilla, Meo, Francesco, Fulia, Antonio, Anania, Valerio, Meli, Antonina, Mondello, Maria Tindara, Raimondo, Viviana, Tulino, Maria Sole, Coletta, Caterina, Cacace
Background Multiple acyl-CoA dehydrogenase deficiency (MADD) or glutaric aciduria type II is an extremely rare autosomal recessive inborn error of fatty acid beta oxidation and branched-chain amino acids, secondary to mutations in the genes encoding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bf6c50e23c1acaec36fe4241daa7240
https://doi.org/10.21203/rs.3.rs-1497075/v1
https://doi.org/10.21203/rs.3.rs-1497075/v1
