| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8274782 | Journal of the Neurological Sciences | 2016 | 5 Pages |
Abstract
Muscular dystrophies can present with rhabdomyolysis; FKRP mutations are particularly frequent in causing such complication. A persistently elevated CK level in patients with rhabdomyolysis warrants consideration for underlying muscular dystrophy.
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Authors
Rajat Lahoria, Margherita Milone,