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Updated: Aug 18, 2026

Behavioral and Locomotor Measurements Using an Open Field Activity Monitoring System for Skeletal Muscle Diseases
Published on: September 29, 2014
LGMD2I presenting with a characteristic Duchenne or Becker muscular dystrophy phenotype
Marianne Schwartz1, Jens Michael Hertz, Marie Louise Sveen
1Department of Clinical Genetics, National University Hospital, Rigshospitalet, Copenhagen, Denmark. schwartz@rh.hosp.dk
Abstract:
LGMD type 2I, caused by mutations in the fukutin-related protein, is a common form of LGMD. The phenotype resembles Duchenne/Becker muscular dystrophy. A point mutation, L276I has been found in all patients with LGMD2I studied so far. The authors screened for this mutation in 102 sporadic cases of Duchenne/Becker mutation-negative patients and found 13 patients with LGMD2I.
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