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Memories of the McNutt fellowship.
Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly.
Pharmacodynamics of fluorouracil-based induction chemotherapy in advanced head and neck cancer.
Detection of facial hypotonia and diagnosis of facioscapulohumeral dystrophy.
Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism.
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Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism.
Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism. Neuron. 2004 Jul 22; 43(2):169-75.
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PubMed
subject areas
Amino Acid Sequence
Cell Line
Dystonia
Humans
Molecular Conformation
Mutation, Missense
Parkinsonian Disorders
Sodium-Potassium-Exchanging ATPase
Structure-Activity Relationship
authors with profiles
William B. Dobyns