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pro vyhledávání: '"Robin Chautard"'
Autor:
Robin Chautard, Cécile Laroche-Raynaud, Anne-Sophie Lia, Pauline Chazelas, Paco Derouault, Franck Sturtz, Yasser Baaj, Alice Veauville-Merllié, Cécile Acquaviva, Frédéric Favreau, Pierre-Antoine Faye
Publikováno v:
BMC Medical Genomics, Vol 13, Iss 1, Pp 1-6 (2020)
Abstract Background Multiple acyl-CoA dehydrogenase deficiency (MADD), previously called glutaric aciduria type II, is a rare congenital metabolic disorder of fatty acids and amino acids oxidation, with recessive autosomal transmission. The prevalenc
Externí odkaz:
https://doaj.org/article/f82f78f6f14a4d479ed7ed90ec0b8056
Autor:
Alice Veauville-Merllié, Pauline Chazelas, Cécile Acquaviva, Yasser Baaj, Anne-Sophie Lia, Frédéric Favreau, Cécile Laroche-Raynaud, Paco Derouault, Franck Sturtz, Robin Chautard, Pierre-Antoine Faye
Publikováno v:
BMC Medical Genomics, Vol 13, Iss 1, Pp 1-6 (2020)
BMC Medical Genomics
BMC Medical Genomics
Background Multiple acyl-CoA dehydrogenase deficiency (MADD), previously called glutaric aciduria type II, is a rare congenital metabolic disorder of fatty acids and amino acids oxidation, with recessive autosomal transmission. The prevalence in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e853ce0092a139a1cb6520123c33a9f3
https://doaj.org/article/f82f78f6f14a4d479ed7ed90ec0b8056
https://doaj.org/article/f82f78f6f14a4d479ed7ed90ec0b8056