Clinical and molecular characterization of limb-girdle muscular dystrophy due to LAMA2 mutations
Research output: Contribution to journal › Journal article › Research › peer-review
In this study we describe the clinical and molecular characteristics of limb-girdle muscular dystrophy (LGMD) due to LAMA2 mutations.
| Original language | English |
|---|---|
| Journal | Muscle & Nerve |
| Volume | 44 |
| Issue number | 5 |
| Pages (from-to) | 703-9 |
| Number of pages | 7 |
| ISSN | 0148-639X |
| DOIs | |
| Publication status | Published - Nov 2011 |
- 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
Research areas
ID: 38425923