157. A novel mutation in LPIN1 gene causing recurrent...

Clinical Neurophysiology 2012 Vol. 123; Iss. 6

157. A novel mutation in LPIN1 gene causing recurrent rhabdomyolysis in childhood: An under-diagnosed condition?

J. Nance, C. Tesi-Rocha, B. Kirmse, K. Raymond
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Volume:
123
Year:
2012
Language:
english
Pages:
1
DOI:
10.1016/j.clinph.2011.11.238
File:
PDF, 39 KB
english, 2012
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