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December 24, 2014Journal of Medical Genetics

ISCA2 mutation causes infantile neurodegenerative mitochondrial disorder

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Authors

ZAZuhair N. Al‐HassnanAlfaisal UniversityMAMazhor AldosaryKing Faisal Specialist Hospital & Research CentreMAMajid AlfadhelKing Saud bin Abdulaziz University for Health Sciences

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Al‐Hassnan et al. (2014) studied this question.

synapsesocial.com/papers/6a71f76a660549caf2c65db5https://doi.org/10.1136/jmedgenet-2014-102592
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