Infantile and Early Childhood Onset of Mitochondrial Myopathy Due to Mutations in the TK2 Gene With a Phenotype of Spinal Muscular Atrophy 5q: The First Cases in Russia

Nervno-Myshechnye Bolezni - Russian Federation
doi 10.17650/2222-8721-2019-9-3-57-76
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Neurology
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Publishing House ABV Press

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