Miyoshi Myopathy Latest Advances

PPMO therapy for dysferlinopathy induces pseudoexon skipping and restoration of functional protein.

Journal: JCI insight

Published: July 14, 2026

Dysferlinopathies: phenotypic study of a Moroccan series of 28 cases.

Journal: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology

Published: January 13, 2026

A novel biallelic mutation in the DYSF gene as a cause of Miyoshi myopathy.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: November 18, 2025

DYSF gene variant spectrum in Arab populations across eight countries: A systematic review.

Journal: Biomolecules & biomedicine

Published: October 25, 2025

An interesting report of POPDC3 limb girdle muscular dystrophy R26 from India.

Journal: Journal of neuromuscular diseases

Published: September 30, 2025

Tips to Design Effective Splice-Switching Antisense Oligonucleotides for Exon Skipping and Exon Inclusion.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: July 28, 2025

An Overview of Recent Advances and Clinical Applications of Exon Skipping and Splice Modulation for Muscular Dystrophy and Various Genetic Diseases.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: July 28, 2025

A Late-Onset Presentation of Miyoshi Myopathy: A Case Report.

Journal: Cureus

Published: July 10, 2025

In Vitro Correction of Point Mutations in the DYSF Gene Using Prime Editing.

Journal: International journal of molecular sciences

Published: April 28, 2025

Dysferlinopathy as cause of long-term hyperCKemia with preserved strength.

Journal: Orphanet journal of rare diseases

Published: March 20, 2025

Whole Exome Sequencing Identified a Stop-Gained Mutation in DYSF Gene Associated With Dysferlinopathy in an Iranian Family.

Journal: International journal of genomics

Published: January 16, 2025

Clinical Presentation, Diagnosis, and Genetic Insights of Miyoshi Myopathy: A Case Report and Literature Review.

Journal: Cureus

Published: September 07, 2024

Miyoshi Myopathy Latest Advances

Find the Latest Research About Miyoshi Myopathy

PPMO therapy for dysferlinopathy induces pseudoexon skipping and restoration of functional protein.

PPMO therapy for dysferlinopathy induces pseudoexon skipping and restoration of functional protein.

Dysferlinopathies: phenotypic study of a Moroccan series of 28 cases.

Dysferlinopathies: phenotypic study of a Moroccan series of 28 cases.

A novel biallelic mutation in the DYSF gene as a cause of Miyoshi myopathy.

A novel biallelic mutation in the DYSF gene as a cause of Miyoshi myopathy.

DYSF gene variant spectrum in Arab populations across eight countries: A systematic review.

DYSF gene variant spectrum in Arab populations across eight countries: A systematic review.

An interesting report of POPDC3 limb girdle muscular dystrophy R26 from India.

An interesting report of POPDC3 limb girdle muscular dystrophy R26 from India.

Tips to Design Effective Splice-Switching Antisense Oligonucleotides for Exon Skipping and Exon Inclusion.

Tips to Design Effective Splice-Switching Antisense Oligonucleotides for Exon Skipping and Exon Inclusion.

An Overview of Recent Advances and Clinical Applications of Exon Skipping and Splice Modulation for Muscular Dystrophy and Various Genetic Diseases.

An Overview of Recent Advances and Clinical Applications of Exon Skipping and Splice Modulation for Muscular Dystrophy and Various Genetic Diseases.

A Late-Onset Presentation of Miyoshi Myopathy: A Case Report.

A Late-Onset Presentation of Miyoshi Myopathy: A Case Report.

In Vitro Correction of Point Mutations in the DYSF Gene Using Prime Editing.

In Vitro Correction of Point Mutations in the DYSF Gene Using Prime Editing.

Dysferlinopathy as cause of long-term hyperCKemia with preserved strength.

Dysferlinopathy as cause of long-term hyperCKemia with preserved strength.

Whole Exome Sequencing Identified a Stop-Gained Mutation in DYSF Gene Associated With Dysferlinopathy in an Iranian Family.

Whole Exome Sequencing Identified a Stop-Gained Mutation in DYSF Gene Associated With Dysferlinopathy in an Iranian Family.

Clinical Presentation, Diagnosis, and Genetic Insights of Miyoshi Myopathy: A Case Report and Literature Review.

Clinical Presentation, Diagnosis, and Genetic Insights of Miyoshi Myopathy: A Case Report and Literature Review.