Effectiveness of whole exome sequencing in unsolved patients with a clinical suspicion of a mitochondrial disorder in Estonia

OBJECTIVE: Reaching a genetic diagnosis of mitochondrial disorders (MDs) is challenging due to their broad phenotypic and genotypic heterogeneity. However, there is growing evidence that the use of whole exome sequencing (WES) for diagnosing patients with a clinical suspicion of an MD is effective (...

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Detalles Bibliográficos
Autores principales: Puusepp, Sanna, Reinson, Karit, Pajusalu, Sander, Murumets, Ülle, Õiglane-Shlik, Eve, Rein, Reet, Talvik, Inga, Rodenburg, Richard J., Õunap, Katrin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043467/
https://www.ncbi.nlm.nih.gov/pubmed/30009132
http://dx.doi.org/10.1016/j.ymgmr.2018.03.004

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6043467/
https://www.ncbi.nlm.nih.gov/pubmed/30009132
http://dx.doi.org/10.1016/j.ymgmr.2018.03.004

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