Kearns-Sayre syndrome is genetically and phenotypically heterogeneous

Josef Finsterer; Sinda Zarrouk-Mahjoub

Kearns-Sayre syndrome is genetically and phenotypically heterogeneous

Josef Finsterer ^{1, *} Sinda Zarrouk-Mahjoub ²

* Corresponding author

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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Journal articles

Domain :

Life Sciences [q-bio]

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Submitted on : Wednesday, February 6, 2019 - 11:26:24 AM
Last modification on : Wednesday, July 3, 2019 - 1:18:26 AM

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Kearns-Sayre syndrome is genetically and phenotypically heterogeneous

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Kearns-Sayre syndrome is genetically and phenotypically heterogeneous

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