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  "authorName": "Taysha Gene Therapies",
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      "text": "SLC13A5 deficiency is caused by mutations in the SLC13A5 gene\nEpileptic episodes start within the first week of life and consists of severe, prolonged episodes\nSevere difficulty with speech production, movement and coordination problems and tooth enamel abnormalities are common\nThe estimated prevalence of SLC13A5 is 225 patients in the US and EU, which is likely higher due to patients being misdiagnosed as cerebral palsy",
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