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Your search keyword '"PKAN disease"' showing total 1 results

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Start Over You searched for: Descriptor "PKAN disease" Remove constraint Descriptor: "PKAN disease" Topic genetic mutation Remove constraint Topic: genetic mutation
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1. Novel Compound Heterozygous Mutation in PANK2 in a Patient with an Atypical Form of Pantothenate Kinase Associated Neurodegeneration and His Family.

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