Molecular Characterization of Exonic Rearrangements and Frame Shifts in the Dystrophin Gene in Duchenne Muscular Dystrophy Patients in a Saudi Community

Human Genomics - United Kingdom
doi 10.1186/s40246-018-0152-8
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Springer Science and Business Media LLC

Related search

Deficiency of Dystrophin-Associated Proteins in Duchenne Muscular Dystrophy Patients Lacking COOH-terminal Domains of Dystrophin.

Journal of Clinical Investigation
Medicine
1993English

Corrigendum: Reading Frame Correction by Targeted Genome Editing Restores Dystrophin Expression in Cells From Duchenne Muscular Dystrophy Patients

Molecular Therapy
Molecular MedicineMolecular BiologyPharmacologyMedicineGeneticsDrug Discovery
2013English

Dystrophin Dp116: A Yet to Be Investigated Product of the Duchenne Muscular Dystrophy Gene

Genes
Genetics
2017English

Dual Exon Skipping in Myostatin and Dystrophin for Duchenne Muscular Dystrophy

BMC Medical Genomics
Genetics
2011English

Immune Responses to Dystrophin: Implications for Gene Therapy of Duchenne Muscular Dystrophy

Gene Therapy
Molecular MedicineGeneticsMolecular Biology
2000English

150. Ex Vivo Gene Therapy of Duchenne Muscular Dystrophy Using iPSCs From Duchenne Muscular Dystrophy Patients

Molecular Therapy
Molecular MedicineMolecular BiologyPharmacologyMedicineGeneticsDrug Discovery
2014English

Duchenne Muscular Dystrophy Gene Therapy: Lost in Translation?

Research and Reports in Biology
2011English

Localisation and Characterisation of Dystrophin in the Central Nervous System of Controls and Patients With Duchenne Muscular Dystrophy.

Journal of Neurology, Neurosurgery and Psychiatry
PsychiatryMental HealthNeurologySurgery
1994English

Becker Muscular Dystrophy in Indian Patients: Analysis of Dystrophin Gene Deletion Patterns

Neurology India
Neurology
2008English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy