Cite
HARVARD Citation
Ozes, B. et al. (2017). PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia. Clinical genetics. 92 (5), pp. 534-539. [Online].
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Ozes, B. et al. (2017). PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia. Clinical genetics. 92 (5), pp. 534-539. [Online].