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New ATP8A2 gene mutations associated with a novel syndrome: encephalopathy, intellectual disability, severe hypotonia, chorea and optic atrophy.

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Description scientific article published on 28 September 2016
Author/s

author: Miguel Angel Martín  Francisco Martínez-Azorín  Antoni Matilla  Marc Corral-Juan  Joaquín Arenas 

Publication date September 28, 2016
Language English
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