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Archive ouverte | Cif, Laura | CCSD

International audience. Abstract Heterozygous mutations in KMT2B are associated with an early-onset, progressive and often complex dystonia (DYT28). Key characteristics of typical disease include focal motor feature...

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Archive ouverte | Acosta, Fernando | CCSD

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Archive ouverte | Thaventhiran, James | CCSD

International audience

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