Modelling of BCS1L-related human mitochondrial disease in Drosophila melanogaster

Mutations in BCS1L are the most frequent cause of human mitochondrial disease linked to complex III deficiency. Different forms of BCS1L-related diseases and more than 20 pathogenic alleles have been reported to date. Clinical symptoms are highly heterogenous, and multisystem involvement is often pr...

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Detalles Bibliográficos
Autores principales: Brischigliaro, Michele, Frigo, Elena, Corrà, Samantha, De Pittà, Cristiano, Szabò, Ildikò, Zeviani, Massimo, Costa, Rodolfo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455400/
https://www.ncbi.nlm.nih.gov/pubmed/34274978
http://dx.doi.org/10.1007/s00109-021-02110-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8455400/
https://www.ncbi.nlm.nih.gov/pubmed/34274978
http://dx.doi.org/10.1007/s00109-021-02110-1

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