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Journal articles
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]
Cited literature [3 references]
https://hal-riip.archives-ouvertes.fr/pasteur-02009260
Contributor : Abdelhakim Ben Hassine Connect in order to contact the contributor
Submitted on : Wednesday, February 6, 2019 - 11:26:24 AM
Last modification on : Wednesday, October 28, 2020 - 9:52:05 AM
Contributor : Abdelhakim Ben Hassine Connect in order to contact the contributor
Submitted on : Wednesday, February 6, 2019 - 11:26:24 AM
Last modification on : Wednesday, October 28, 2020 - 9:52:05 AM
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