ATP1A3 mutations: What is the phenotype?

Allison Brashear; Laurie J. Ozelius; Kathleen J. Sweadner

doi:10.1212/WNL.0000000000000113

ATP1A3 mutations: What is the phenotype?

Allison Brashear
, Laurie J. Ozelius
, Kathleen J. Sweadner

JSMBS Office of the Dean

Icahn School of Medicine at Mount Sinai
Massachusetts General Hospital

Research output: Contribution to journal › Editorial

11 Scopus citations

Original language	English
Pages (from-to)	468-469
Number of pages	2
Journal	Neurology
Volume	82
Issue number	6
DOIs	https://doi.org/10.1212/WNL.0000000000000113
State	Published - Feb 11 2014

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@article{9a51d99e1a634a38bee3812b26960bb2,

title = "ATP1A3 mutations: What is the phenotype?",

author = "Allison Brashear and Ozelius, \{Laurie J.\} and Sweadner, \{Kathleen J.\}",

year = "2014",

month = feb,

day = "11",

doi = "10.1212/WNL.0000000000000113",

language = "English",

volume = "82",

pages = "468--469",

journal = "Neurology",

issn = "0028-3878",

publisher = "Lippincott Williams and Wilkins",

number = "6",

}

TY - JOUR

T1 - ATP1A3 mutations

T2 - What is the phenotype?

AU - Brashear, Allison

AU - Ozelius, Laurie J.

AU - Sweadner, Kathleen J.

PY - 2014/2/11

Y1 - 2014/2/11

UR - https://www.scopus.com/pages/publications/84895736198

U2 - 10.1212/WNL.0000000000000113

DO - 10.1212/WNL.0000000000000113

M3 - Editorial

C2 - 24431297

AN - SCOPUS:84895736198

SN - 0028-3878

VL - 82

SP - 468

EP - 469

JO - Neurology

JF - Neurology

IS - 6

ER -

ATP1A3 mutations: What is the phenotype?

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