Mitochondrial dysfunction in down syndrome: molecular mechanisms and therapeutic targets

Trisomy of chromosome 21 (TS21) is the most common autosomal aneuploidy compatible with postnatal survival with a prevalence of 1 in 700 newborns. Its phenotype is highly complex with constant features, such as mental retardation, dysmorphic traits and hypotonia, and variable features including hear...

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Detalles Bibliográficos
Publicado en:Mol Med
Main Authors: Izzo, Antonella, Mollo, Nunzia, Nitti, Maria, Paladino, Simona, Calì, Gaetano, Genesio, Rita, Bonfiglio, Ferdinando, Cicatiello, Rita, Barbato, Maria, Sarnataro, Viviana, Conti, Anna, Nitsch, Lucio
Formato: Artigo
Idioma:Inglês
Publicado: BioMed Central 2018
Assuntos:
Review
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6016872/
https://ncbi.nlm.nih.gov/pubmed/30134785
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s10020-018-0004-y
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