Mitochondrial DNA variants in inclusion body myositis characterized by deep sequencing-Reference-Cited by-同舟云学术

Mitochondrial DNA variants in inclusion body myositis characterized by deep sequencing

Published:2021-05 Issue:3 Volume:31 Page:
ISSN:1015-6305
Container-title:Brain Pathology
language:en
Short-container-title:Brain Pathology

Author:

Hedberg‐Oldfors Carola¹^ORCID,Lindgren Ulrika¹²^ORCID,Basu Swaraj³^ORCID,Visuttijai Kittichate¹^ORCID,Lindberg Christopher²^ORCID,Falkenberg Maria³^ORCID,Larsson Lekholm Erik³^ORCID,Oldfors Anders¹^ORCID

Affiliation:

1. Department of Laboratory Medicine University of Gothenburg Gothenburg Sweden

2. Neuromuscular Centre Department of Neurology Sahlgrenska University Hospital Gothenburg Sweden

3. Department of Medical Biochemistry and Cell Biology University of Gothenburg Gothenburg Sweden

Funder

Vetenskapsrådet

Publisher

Wiley

Subject

Clinical Neurology,Pathology and Forensic Medicine,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bpa.12931

Reference40 articles.

1. Inclusion body myositis

2. Long-term observational study of sporadic inclusion body myositis

3. Inclusion body myositis: clinical features and pathogenesis

4. Inclusion body myositis: clinical, morphological, physiological and laboratory findings in 18 cases

5. Inclusion body myositis: A review of clinical and genetic aspects, diagnostic criteria and therapeutic approaches

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