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HARVARD Citation
Zulfiqar, S. et al. (2019). Whole exome sequencing identifies novel variant underlying hereditary spastic paraplegia in consanguineous Pakistani families. Journal of clinical neuroscience. pp. 19-23. [Online].
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Zulfiqar, S. et al. (2019). Whole exome sequencing identifies novel variant underlying hereditary spastic paraplegia in consanguineous Pakistani families. Journal of clinical neuroscience. pp. 19-23. [Online].