Case report of cerebral creatine deficiency syndrome with novel mutation of SLC6A8 gene in a male child in Bangladesh

Muhammad Mizanur Rahman, Kanij Fatema

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https://doi.org/10.5734/jgm.2021.18.1.44

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Journal: Journal of Genetic Medicine	Publication Date: Jun 30, 2021
License type: CC BY-NC 4.0

Abstract

Case report of cerebral creatine deficiency syndrome with novel mutation of <i>SLC6A8</i> gene in a male child in Bangladesh

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