A novel WDR45 mutation in a patient with β-propeller protein-associated neurodegeneration

Ítems similars

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• A novel WDR45 mutation in a patient with static encephalopathy of childhood with neurodegeneration in adulthood (SENDA)
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• A Case of Beta-propeller Protein-associated Neurodegeneration due to a Heterozygous Deletion of WDR45
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• Is WDR45 the missing link for ER stress-induced autophagy in beta-propeller associated neurodegeneration?
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• WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype
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