Effectiveness of clinical exome sequencing in adult patients with difficult‐to‐diagnose neurological disorders-Reference-Cited by-同舟云学术

Effectiveness of clinical exome sequencing in adult patients with difficult‐to‐diagnose neurological disorders

Published:2021-08-21 Issue:1 Volume:145 Page:63-72
ISSN:0001-6314
Container-title:Acta Neurologica Scandinavica
language:en
Short-container-title:Acta Neuro Scandinavica

Author:

Sainio Markus T.¹^ORCID,Aaltio Juho¹,Hyttinen Virva²³,Kortelainen Mika²⁴,Ojanen Simo⁵,Paetau Anders⁶,Tienari Pentti⁷⁸,Ylikallio Emil¹⁷,Auranen Mari⁷,Tyynismaa Henna¹⁹¹⁰

Affiliation:

1. Stem Cells and Metabolism Research Program Faculty of Medicine University of Helsinki Helsinki Finland

2. VATT Institute for Economic Research Helsinki Finland

3. Department of Health and Social Management University of Eastern Finland Kuopio Finland

4. Department of Economics Turku School of Economics Turku Finland

5. Department of Veterinary Biosciences Faculty of Veterinary Medicine University of Helsinki Helsinki Finland

6. Department of Pathology HUSLAB and University of Helsinki Helsinki Finland

7. Clinical Neurosciences Neurology University of Helsinki and Helsinki University Hospital Helsinki Finland

8. Translational Immunology Research Program Faculty of Medicine University of Helsinki Helsinki Finland

9. Department of Medical and Clinical Genetics University of Helsinki Helsinki Finland

10. Neuroscience Center Helsinki Institute of Life Science University of Helsinki Helsinki Finland

Funder

Biomedicum Helsinki-säätiö

Publisher

Wiley

Subject

Neurology (clinical),Neurology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ane.13522

Reference45 articles.

1. Clinical application of next-generation sequencing to the practice of neurology

2. Targeted next-generation sequencing panels in the diagnosis of Charcot-Marie-Tooth disease

3. Next-generation sequencing in Charcot–Marie–Tooth disease: opportunities and challenges

4. Targeted next-generation sequencing reveals further genetic heterogeneity in axonal Charcot–Marie–Tooth neuropathy and a mutation in HSPB1

5. Hereditary spastic paraplegia: from diagnosis to emerging therapeutic approaches

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