Alpha-sarcoglycanopathy presenting as exercise intolerance and rhabdomyolysis in two adults
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
Reference17 articles.
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3. Pseudo-metabolic presentation in a Duchenne muscular dystrophy symptomatic carrier with ‘de novo’ duplication of dystrophin gene;Romero;Neuromuscul Disord,2001
4. Alpha-sarcoglycan deficiency featuring exercise intolerance and myoglobinuria;Mongini;Neuropediatrics,2002
5. Myoglobinuria as first clinical sign of a primary alpha-sarcoglycanopathy;Ceravolo;Eur J Pediatr,2014
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