Research
Print page Print page
Switch language
The Capital Region of Denmark - a part of Copenhagen University Hospital
Published

Clinical and molecular characterization of limb-girdle muscular dystrophy due to LAMA2 mutations

Research output: Contribution to journalJournal articleResearchpeer-review

DOI

  1. Molecular indicators of denervation in aging human skeletal muscle

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Moderate-intensity aerobic exercise improves physical fitness in bethlem myopathy

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Long-term safety and efficacy of eculizumab in generalized myasthenia gravis

    Research output: Contribution to journalJournal articleResearchpeer-review

  1. Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry)

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Phenotypic Spectrum of α-Dystroglycanopathies Associated With the c.919T>a Variant in the FKRP Gene in Humans and Mice

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Bimagrumab vs Optimized Standard of Care for Treatment of Sarcopenia in Community-Dwelling Older Adults: A Randomized Clinical Trial

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Vacuoles, Often Containing Glycogen, Are a Consistent Finding in Hypokalemic Periodic Paralysis

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Editorial: Remaining diagnostic issues and start of a treatment era for muscle diseases

    Research output: Contribution to journalJournal articleResearchpeer-review

View graph of relations
In this study we describe the clinical and molecular characteristics of limb-girdle muscular dystrophy (LGMD) due to LAMA2 mutations.
Original languageEnglish
JournalMuscle & Nerve
Volume44
Issue number5
Pages (from-to)703-9
Number of pages7
ISSN0148-639X
DOIs
Publication statusPublished - 2011

    Research areas

  • Adolescent, Aged, Alternative Splicing, Base Sequence, Child, Female, Humans, Laminin, Male, Middle Aged, Molecular Sequence Data, Muscular Dystrophies, Limb-Girdle, Mutagenesis, Insertional, Mutation, Phenotype, RNA Splice Sites, Young Adult

ID: 33192883