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APA Citation
Ueda, M., Kawamura, N., Tateishi, T., Sakae, N., Motomura, K., Ohyagi, Y., & Kira, J. (2010). phenotypic spectrum of hereditary neuralgic amyotrophy caused by the SEPT9 R88W mutation. Journal of neurology, neurosurgery and psychiatry, 81(1), 94–96. http://access.bl.uk/ark:/81055/vdc_100137791889.0x000039