Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Ester Simon Borges"'
Autor:
Adriana Aparecida Marques, Gabriela Castro, Greice Andreotti de Molfetta, Daniel F. Garcia, Ester Simon Borges, Valerie Hamilton, Wilson A. Silva, Ida Vanessa Doederlein Schwartz, Ana Vitoria Barban Margutti, Verónica Cornejo, José Simon Camelo, Fernanda Sperb-Ludwig, Diana Ruffato Resende Campanholi
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 9, Iss 5, Pp n/a-n/a (2021)
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Molecular Genetics & Genomic Medicine, Vol 9, Iss 5, Pp n/a-n/a (2021)
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Background Maple syrup urine disease (MSUD) is an autosomal recessive inherited metabolic disorder caused by the deficient activity of the branched‐chain α‐keto acid dehydrogenase (BCKD) enzymatic complex. BCKD is a mitochondrial complex encoded
Autor:
Gabriela Castro, Diana Ruffato Resende Campanholi, Verónica Cornejo, Valerie Hamilton, José Simon Camelo Júnior, Wilson A. Silva, Greice Andreotti de Molfetta, Adriana Aparecida Marques, Ester Simon Borges, Daniel F. Garcia, Ana Vitoria Barban Margutti, Ida Vanessa Doederlein Schwartz
Background: Maple syrup urine disease (MSUD) is an autosomal recessive inherited metabolic disorder caused by the deficient activity of the branched-chain α-keto acid dehydrogenase (BCKD) enzymatic complex. BCKD is a mitochondrial complex encoded by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b64f530b076c4497d7b29f9665170dd
https://doi.org/10.21203/rs.2.18080/v2
https://doi.org/10.21203/rs.2.18080/v2
Autor:
Diana Ruffato Resende Campanholi, Ana Vitoria Barban Margutti, Wilson Araújo Silva, Daniel Fantozzi Garcia, Greice Andreotti de Molfetta, Adriana Aparecida Marques, Ida Vanessa Döederlein Schwartz, Veronica Cornejo, Valerie Hamilton, Gabriela Castro, Ester Simon Borges, José Simon Camelo Junior
Background: Maple syrup urine disease (MSUD) is an autosomal recessive inherited metabolic disease caused by deficient activity of the branched-chain α-keto acid dehydrogenase (BCKD) enzymatic complex. BCKD is a mitochondrial complex encoded by four
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d7548a87fb5207e1399e81fea8ee780
https://doi.org/10.21203/rs.2.18080/v1
https://doi.org/10.21203/rs.2.18080/v1