Zobrazeno 1 - 2
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pro vyhledávání: '"Melania González-Torres"'
Autor:
Alejandro Gella, Patricia Prada-Dacasa, Montserrat Carrascal, Andrea Urpi, Melania González-Torres, Joaquin Abian, Elisenda Sanz, Albert Quintana
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 8 (2020)
Defects in mitochondrial function lead to severe neuromuscular orphan pathologies known as mitochondrial disease. Among them, Leigh Syndrome is the most common pediatric presentation, characterized by symmetrical brain lesions, hypotonia, motor and r
Externí odkaz:
https://doaj.org/article/2ee59d68877041839468b29143c278fb
Autor:
Alejandro Gella, Elisenda Sanz, Joaquín Abián, Albert Quintana, Patricia Prada-Dacasa, Melania González-Torres, Montserrat Carrascal
Defects in mitochondrial function lead to severe neuromuscular orphan pathologies known as mitochondrial disease. Among them, Leigh Syndrome is the most common pediatric presentation, characterized by symmetrical brain lesions, hypotonia, motor and r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4efe46f3f4df5a9dd668e725ef7b842c
