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HARVARD Citation
Torraco, A. et al. (n.d.). ISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe–4S] proteins. Human molecular genetics. p. 3650. [Online].
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Torraco, A. et al. (n.d.). ISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe–4S] proteins. Human molecular genetics. p. 3650. [Online].