Kearns-Sayre syndrome is genetically and phenotypically heterogeneous

Abstract : Letter to the Editor Comment on : Kearns-Sayre syndrome with facial and white matter extensive involvement: a (mitochondrial and nuclear gene related?) neurocristopathy? [Pediatr Med Chir. 2017]
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Josef Finsterer, Sinda Zarrouk-Mahjoub. Kearns-Sayre syndrome is genetically and phenotypically heterogeneous. Pediatria Medica e Chirurgica, Pediatria Medica e Chirurgica, 2018, 40 (1), ⟨10.4081/pmc.2018.193⟩. ⟨pasteur-02009260⟩

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