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Publications by Eleonora Lamantea
Lack of the Mitochondrial Protein Acylglycerol Kinase Causes Sengers Syndrome
American Journal of Human Genetics
Genetics
VARS2andTARS2Mutations in Patients With Mitochondrial Encephalomyopathies
Human Mutation
Genetics
Expanded Spectrum of Pelizaeus–Merzbacher-Like Disease: Literature Revision and Description of a Novel GJC2 Mutation in an Unusually Severe Form
European Journal of Human Genetics
Genetics
Assessment of the Retinal Posterior Pole in Dominant Optic Atrophy by Spectral-Domain Optical Coherence Tomography and Microperimetry
PLoS ONE
Multidisciplinary
Epilepsy in Mitochondrial Disorders
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