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TK2-related Myopathic Mitochondrial Depletion Syndrome

Abstract : Letter to the Editor Comment on : Myopathic mtDNA Depletion Syndrome Due to Mutation in TK2 Gene. [Pediatr Dev Pathol. 2017]
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https://hal-riip.archives-ouvertes.fr/pasteur-02010359
Contributor : Abdelhakim Ben Hassine <>
Submitted on : Thursday, February 7, 2019 - 10:21:18 AM
Last modification on : Friday, October 23, 2020 - 6:48:04 PM

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Josef Finsterer, Sinda Zarrouk-Mahjoub. TK2-related Myopathic Mitochondrial Depletion Syndrome. Pediatric and developmental pathology, Springer Verlag, 2018, 21 (5), pp.507-508. ⟨10.1177/1093526617743906⟩. ⟨pasteur-02010359⟩

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