Cite
HARVARD Citation
Wen, B. et al. (2010). Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations. Journal of neurology, neurosurgery and psychiatry. 81 (2), pp. 231-236. [Online].
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Wen, B. et al. (2010). Riboflavin-responsive lipid-storage myopathy caused by ETFDH gene mutations. Journal of neurology, neurosurgery and psychiatry. 81 (2), pp. 231-236. [Online].