Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Mattia, Pellas"'
Autor:
Livia Cosentino, Chiara Urbinati, Chiara Lanzillotta, Domenico De Rasmo, Daniela Valenti, Mattia Pellas, Maria Cristina Quattrini, Fabiana Piscitelli, Magdalena Kostrzewa, Fabio Di Domenico, Donatella Pietraforte, Tiziana Bisogno, Anna Signorile, Rosa Anna Vacca, Bianca De Filippis
Publikováno v:
Molecular Autism, Vol 15, Iss 1, Pp 1-14 (2024)
Abstract Background Defective mitochondria and aberrant brain mitochondrial bioenergetics are consistent features in syndromic intellectual disability disorders, such as Rett syndrome (RTT), a rare neurologic disorder that severely affects mainly fem
Externí odkaz:
https://doaj.org/article/8f0a63e3f3f04232b7cd24a12f9c6f55
Autor:
Urbinati, Chiara, Livia, Cosentino, Daniela, Valenti, Domenico De Rasmo, Anna, Signorile, Mattia, Pellas, Rosa Anna Vacca, Bianca De Filippis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3686::136534a76ad7ff06e8cae2e51db0bd9f
https://hdl.handle.net/11573/1672899
https://hdl.handle.net/11573/1672899
Publikováno v:
Neuroscience. 453
Rett syndrome (RTT) is a rare neurologic disorder, characterized by severe behavioural and physiological symptoms. RTT is caused by mutations in the MECP2 gene in about 95% of cases and to date no cure is available. Recent evidence suggests that non-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c5c17826578c27aeacf7a89869392e7
https://pubmed.ncbi.nlm.nih.gov/33010341
https://pubmed.ncbi.nlm.nih.gov/33010341