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]
https://hal-riip.archives-ouvertes.fr/pasteur-02009260
Contributor : Abdelhakim Ben Hassine <>
Submitted on : Wednesday, February 6, 2019 - 11:26:24 AM Last modification on : Wednesday, October 28, 2020 - 9:52:05 AM
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⟩