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HARVARD Citation
Abbas, S. et al. (2021). Exome sequencing of a Pakistani family with spastic paraplegia identified an 18 bp deletion in the cytochrome B5 domain of FA2H. Neurological research. pp. 133-140. [Online].
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Abbas, S. et al. (2021). Exome sequencing of a Pakistani family with spastic paraplegia identified an 18 bp deletion in the cytochrome B5 domain of FA2H. Neurological research. pp. 133-140. [Online].