Pathologic Variability Associated With Phenotypic Differences in Siblings With ACTA1 Myopathy

Journal article

Peer reviewed

Robert Kiss, Steven A Moore, Vikki Stefans, Murat Gokden and Aravindhan Veerapandiyan

Muscle & nerve

02/21/2026

DOI: 10.1002/mus.70187

PMID: 41721548

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no abstract | case report

Phenotype

cytoplasmic body

ACTA1

nemaline rods

congenital myopathy

Title: Subtitle: Pathologic Variability Associated With Phenotypic Differences in Siblings With ACTA1 Myopathy
Creators: Robert Kiss - Arkansas Children's Hospital
Steven A Moore - University of Iowa
Vikki Stefans - Arkansas Children's Hospital
Murat Gokden - University of Arkansas for Medical Sciences
Aravindhan Veerapandiyan - Arkansas Children's Hospital
Resource Type: Journal article
Publication Details: Muscle & nerve
DOI: 10.1002/mus.70187
PMID: 41721548
NLM abbreviation: Muscle Nerve
ISSN: 0148-639X
eISSN: 1097-4598
Publisher: Wiley
Language: English
Electronic publication date: 02/21/2026
Academic Unit: Pathology
Record Identifier: 9985139312402771

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