Cargando…
Minisequencing mitochondrial DNA pathogenic mutations
BACKGROUND: There are a number of well-known mutations responsible of common mitochondrial DNA (mtDNA) diseases. In order to overcome technical problems related to the analysis of complete mtDNA genomes, a variety of different techniques have been proposed that allow the screening of coding region p...
Autores principales: | Álvarez-Iglesias, Vanesa, Barros, Francisco, Carracedo, Ángel, Salas, Antonio |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2377236/ https://www.ncbi.nlm.nih.gov/pubmed/18402672 http://dx.doi.org/10.1186/1471-2350-9-26 |
Ejemplares similares
-
Reassessing the role of mitochondrial DNA mutations in autism spectrum disorder
por: Álvarez-Iglesias, Vanesa, et al.
Publicado: (2011) -
Application of hybridization control probe to increase accuracy on ligation detection or minisequencing diagnostic microarrays
por: Ritari, Jarmo, et al.
Publicado: (2009) -
A decision tree to improve identification of pathogenic mutations in clinical practice
por: do Nascimento, Priscilla Machado, et al.
Publicado: (2020) -
Multiple strand displacement amplification of mitochondrial DNA from clinical samples
por: Maragh, Samantha, et al.
Publicado: (2008) -
Identification of Avramr1 from Phytophthora infestans using long read and cDNA pathogen‐enrichment sequencing (PenSeq)
por: Lin, Xiao, et al.
Publicado: (2020)