Kearns-Sayre syndrome is genetically and phenotypically heterogeneous
Résumé
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]
Domaines
Sciences du Vivant [q-bio]
Origine : Publication financée par une institution
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