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Journal articles

Kearns-Sayre syndrome is genetically and phenotypically heterogeneous

Josef Finsterer 1, * Sinda Zarrouk-Mahjoub 2 
* Corresponding author
1 Krankenanstalt Rudolfstiftung
2 LR11IPT05 - Laboratoire de Génomique Biomédicale et Oncogénétique - Biomedical Genomics and Oncogenetics Laboratory
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]
Keywords : Kearns-Sayre syndrome mtDNA Leucoencephalopathy Phenotype Genotype
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Submitted on : Wednesday, February 6, 2019 - 11:26:24 AM
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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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