Recurrent rhabdomyolysis and an autosomal dominant family history of scoliosis: clinical features leading to a diagnosis of metabolic myopathy

Authors

DOI:

https://doi.org/10.17161/rrnmf.v3i3.16318

Keywords:

RYR1, Scoliosis, Rhabdomyolysis

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Published

2022-09-26

How to Cite

Wright, S., & Brady, S. (2022). Recurrent rhabdomyolysis and an autosomal dominant family history of scoliosis: clinical features leading to a diagnosis of metabolic myopathy. RRNMF Neuromuscular Journal, 3(3), 10. https://doi.org/10.17161/rrnmf.v3i3.16318

Issue

Section

Clinic Stuff (Case Reports)