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Dive into the research topics of 'Mild myopathic phenotype in a patient with homozygous c.416C > T mutation in TK2 gene'. Together they form a unique fingerprint.- Sort by
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George K Papadimas, Efthimia Vargiami, Pinelopi Dragoumi, Rudy Van Coster, Joel Smet, Sara Seneca, Constantinos Papadopoulos, Evangelia Kararizou, Dimitrios Zafeiriou
Research output: Contribution to journal › Article › peer-review