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Novel mouse model reveals the mechanisms of a rare genetic encephalopathy
A team at the Centre de recherche Azrieli du CHU Sainte-Justine has reached a major milestone in understanding a rare and severe form of genetic encephalopathy associated with the DHDDS gene.
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Researchers at the Centre de recherche Azrieli du CHU Sainte‑Justine reported a major milestone in deciphering the mechanisms of a rare, severe genetic encephalopathy linked to the DHDDS gene.
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