Abstract|Topic: 7 - Neuromuscular disorders| Volume 333, SUPPLEMENT 1, e428-e429, October 15, 2013

LGMD2I: Immunohistochemical and immunoblot technique assisted identification of 51 cases with both duchenne and becker phenotype

      Background: LGMD 2I is caused by mutations in fukutin-related protein gene (FKRP).
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