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P266 – 2077 AADC deficiency with oculogyric crises as the most specific presenting symptom

Year: 2013

Type: conference-abstract

Source: European Journal of Paediatric Neurology

DOI: 10.1016/s1090-3798(13)70445-8

Authors: G de Bruyn, L Régal, L Wouters, K Jansen, G Buyse, L Lagae

Language: English

Topic: Metabolism and Genetic Disorders

Subfield: Clinical Biochemistry

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2319284302

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