A Naturally Occurring Human Minidysferlin Protein Repairs Sarcolemmal Lesions in a Mouse Model of Dysferlinopathy

Efficient recovery of dysferlin deficiency by dual adeno-associated vector-mediated gene transfer

(2010) William Lostal et al.   HUMAN MOLECULAR GENETICS

Dysferlin associates with the developing T-tubule system in rodent and human skeletal muscle

(2010) Lars Klinge et al.   MUSCLE & NERVE

Genetic Manipulation of Dysferlin Expression in Skeletal Muscle

(2009) Douglas P. Millay et al.   AMERICAN JOURNAL OF PATHOLOGY

Identification of Different Genomic Deletions and One Duplication in the Dysferlin Gene Using Multiplex Ligation-Dependent Probe Amplification and Genomic Quantitative PCR

(2009) Martin Krahn et al.   Genetic Testing and Molecular Biomarkers

Theoretic applicability of antisense-mediated exon skipping for Duchenne muscular dystrophy mutations

(2009) Annemieke Aartsma-Rus et al.   HUMAN MUTATION

Efficient bypass of mutations in dysferlin deficient patient cells by antisense-induced exon skipping

(2009) Nicolas Wein et al.   HUMAN MUTATION

Intravenous Administration of Self-complementary AAV9 Enables Transgene Delivery to Adult Motor Neurons

(2009) Sandra Duque et al.   MOLECULAR THERAPY

How to go about diagnosing and managing the limb-girdle muscular dystrophies

(2009) Kate Bushby et al.   NEUROLOGY INDIA

Immunolabelling and flow cytometry as new tools to explore dysferlinopathies

(2009) N. Wein et al.   NEUROMUSCULAR DISORDERS

Detection of exonic copy-number changes using a highly efficient oligonucleotide-based comparative genomic hybridization-array method

(2008) Yoann Saillour et al.   HUMAN MUTATION

Analysis of theDYSFmutational spectrum in a large cohort of patients

(2008) Martin Krahn et al.   HUMAN MUTATION