New perspective in diagnostics of mitochondrial disorders: two years’ experience with whole-exome sequencing at a national paediatric centre

BACKGROUND: Whole-exome sequencing (WES) has led to an exponential increase in identification of causative variants in mitochondrial disorders (MD). METHODS: We performed WES in 113 MD suspected patients from Polish paediatric reference centre, in whom routine testing failed to identify a molecular...

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Detalles Bibliográficos
Autores principales: Pronicka, Ewa, Piekutowska-Abramczuk, Dorota, Ciara, Elżbieta, Trubicka, Joanna, Rokicki, Dariusz, Karkucińska-Więckowska, Agnieszka, Pajdowska, Magdalena, Jurkiewicz, Elżbieta, Halat, Paulina, Kosińska, Joanna, Pollak, Agnieszka, Rydzanicz, Małgorzata, Stawinski, Piotr, Pronicki, Maciej, Krajewska-Walasek, Małgorzata, Płoski, Rafał
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4903158/
https://www.ncbi.nlm.nih.gov/pubmed/27290639
http://dx.doi.org/10.1186/s12967-016-0930-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4903158/
https://www.ncbi.nlm.nih.gov/pubmed/27290639
http://dx.doi.org/10.1186/s12967-016-0930-9

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