A wide clinical phenotype spectrum in patients with ATP1A2 mutations.
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ATP1A2 Mutations in Migraine: Seeing through the Facets of an Ion Pump onto the Neurobiology of DiseaseEpilepsy in hemiplegic migraine: Genetic mutations and clinical implications.Genetic Variants Associated with Episodic Ataxia in Korea.More Than a Decade of Misdiagnosis of Alternating Hemiplegia of Childhood with Catastrophic Outcome.More Than a Decade of Misdiagnosis of Alternating Hemiplegia of Childhood with Catastrophic Outcome.
P2860
A wide clinical phenotype spectrum in patients with ATP1A2 mutations.
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2013 nî lūn-bûn
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A wide clinical phenotype spectrum in patients with ATP1A2 mutations.
@en
A wide clinical phenotype spectrum in patients with ATP1A2 mutations.
@nl
type
label
A wide clinical phenotype spectrum in patients with ATP1A2 mutations.
@en
A wide clinical phenotype spectrum in patients with ATP1A2 mutations.
@nl
prefLabel
A wide clinical phenotype spectrum in patients with ATP1A2 mutations.
@en
A wide clinical phenotype spectrum in patients with ATP1A2 mutations.
@nl
P2093
P2860
P356
P1476
A wide clinical phenotype spectrum in patients with ATP1A2 mutations.
@en
P2093
Amal Al-Hashem
Bashaer Al-Bulushi
Brahim Tabarki
P2860
P304
P356
10.1177/0883073813504623
P577
2013-10-04T00:00:00Z