Myofibrillar myopathy presenting with an inclusion body<scp>myositis‐like</scp>phenotype-Reference-Cited by-同舟云学术

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Myofibrillar myopathy presenting with an inclusion bodymyositis‐likephenotype

Published:2023-03-07 Issue:5 Volume:67 Page:
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle and Nerve

Author:

Diaz Frank¹²^ORCID,Soltanzadeh Payam³,Khosa Shaweta²³,Khanlou Negar⁴,Freundlich Robert²,Mishra Shri K.²³⁵

Affiliation:

1. Department of Neurology Cedars‐Sinai Medical Center Los Angeles California USA

2. Department of Neurology Olive View‐UCLA Medical Center Sylmar California USA

3. Department of Neurology David Geffen School of Medicine at UCLA Los Angeles California USA

4. Department of Pathology David Geffen School of Medicine at UCLA Los Angeles California USA

5. Department of Neurology Keck School of Medicine Los Angeles California USA

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mus.27806

Reference7 articles.

1. Myofibrillar Myopathies: A Clinical and Myopathological Guide

2. Inclusion body myositis: clinical features and pathogenesis

3. Myopathies with finger flexor weakness: Not only inclusion‐body myositis

4. The p.G154S mutation of the alpha-B crystallin gene (CRYAB) causes late-onset distal myopathy

5. Familial inclusion body myositis with negative anti‐cytosolic 5′‐nucleotidase 1A (CN1A) antibody test;Khosa S;Neurology.,2019

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