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]
Journal Articles
Pediatric and developmental pathology
Year : 2018
AbdelHakim Ben Hassine : Connect in order to contact the contributor
https://hal-riip.archives-ouvertes.fr/pasteur-02010359
Submitted on : Thursday, February 7, 2019-10:21:18 AM
Last modification on : Wednesday, October 28, 2020-9:52:05 AM
Dates and versions
Identifiers
- HAL Id : pasteur-02010359 , version 1
- DOI : 10.1177/1093526617743906
- PUBMED : 29173062
Cite
Josef Finsterer, Sinda Zarrouk-Mahjoub. TK2-related Myopathic Mitochondrial Depletion Syndrome. Pediatric and developmental pathology, 2018, 21 (5), pp.507-508. ⟨10.1177/1093526617743906⟩. ⟨pasteur-02010359⟩
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