Cost-effectiveness of massively parallel sequencing for diagnosis of paediatric muscle diseases

Abstract Childhood-onset muscle disorders are genetically heterogeneous. Diagnostic workup has traditionally included muscle biopsy, protein-based studies of muscle specimens, and candidate gene sequencing. High throughput or massively parallel sequencing is transforming the approach to diagnosis of...

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Auteurs principaux: Deborah Schofield, Khurshid Alam, Lyndal Douglas, Rupendra Shrestha, Daniel G. MacArthur, Mark Davis, Nigel G. Laing, Nigel F. Clarke, Joshua Burns, Sandra T. Cooper, Kathryn N. North, Sarah A. Sandaradura, Gina L. O’Grady
Format: article
Langue:EN
Publié: Nature Portfolio 2017
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R
Accès en ligne:https://doaj.org/article/7b114791b2e44d7cabd2c2fc9832f309
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