D-DEMO, A Novel and Distinct Phenotype Caused by ATP1A3 Mutations
Conferences
Prange, L; Shashi, V; Herman, K; Schiffmann, R; Abdelnour, E; Jasien, J; Kansagra, S; McLean, M; Walley, N; Azar, A; Heinzen, E; Mikati, M
Published in: NEUROLOGY
April 18, 2017
Duke Scholars
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Published In
NEUROLOGY
EISSN
1526-632X
ISSN
0028-3878
Publication Date
April 18, 2017
Volume
88
Related Subject Headings
- Neurology & Neurosurgery
- 3209 Neurosciences
- 3202 Clinical sciences
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Prange, L., Shashi, V., Herman, K., Schiffmann, R., Abdelnour, E., Jasien, J., … Mikati, M. (2017). D-DEMO, A Novel and Distinct Phenotype Caused by ATP1A3 Mutations. In NEUROLOGY (Vol. 88).
Prange, Lyndsey, Vandana Shashi, Kristin Herman, Raphael Schiffmann, Elie Abdelnour, Joan Jasien, Sujay Kansagra, et al. “D-DEMO, A Novel and Distinct Phenotype Caused by ATP1A3 Mutations.” In NEUROLOGY, Vol. 88, 2017.
Prange L, Shashi V, Herman K, Schiffmann R, Abdelnour E, Jasien J, et al. D-DEMO, A Novel and Distinct Phenotype Caused by ATP1A3 Mutations. In: NEUROLOGY. 2017.
Prange, Lyndsey, et al. “D-DEMO, A Novel and Distinct Phenotype Caused by ATP1A3 Mutations.” NEUROLOGY, vol. 88, 2017.
Prange L, Shashi V, Herman K, Schiffmann R, Abdelnour E, Jasien J, Kansagra S, McLean M, Walley N, Azar A, Heinzen E, Mikati M. D-DEMO, A Novel and Distinct Phenotype Caused by ATP1A3 Mutations. NEUROLOGY. 2017.
Published In
NEUROLOGY
EISSN
1526-632X
ISSN
0028-3878
Publication Date
April 18, 2017
Volume
88
Related Subject Headings
- Neurology & Neurosurgery
- 3209 Neurosciences
- 3202 Clinical sciences