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Editorial
. 2014 Feb 11;82(6):468-9.
doi: 10.1212/WNL.0000000000000113. Epub 2014 Jan 15.

ATP1A3 mutations: what is the phenotype?

Allison Brashear  1 , Laurie J Ozelius, Kathleen J Sweadner
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Editorial

ATP1A3 mutations: what is the phenotype?

Allison Brashear et al. Neurology. .
No abstract available

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  • Genotype-phenotype correlations in alternating hemiplegia of childhood.
    Sasaki M, Ishii A, Saito Y, Morisada N, Iijima K, Takada S, Araki A, Tanabe Y, Arai H, Yamashita S, Ohashi T, Oda Y, Ichiseki H, Hirabayashi S, Yasuhara A, Kawawaki H, Kimura S, Shimono M, Narumiya S, Suzuki M, Yoshida T, Oyazato Y, Tsuneishi S, Ozasa S, Yokochi K, Dejima S, Akiyama T, Kishi N, Kira R, Ikeda T, Oguni H, Zhang B, Tsuji S, Hirose S. Sasaki M, et al. Neurology. 2014 Feb 11;82(6):482-90. doi: 10.1212/WNL.0000000000000102. Epub 2014 Jan 15. Neurology. 2014. PMID: 24431296

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