D-DEMØ, a distinct phenotype caused by ATP1A3 mutations.
Prange L, Pratt M, Herman K, Schiffmann R, Mueller DM, McLean M, Mendez MM, Walley N, Heinzen EL, Goldstein D, Shashi V, Hunanyan A, Pagadala V, Mikati MA.
Prange L, et al. Among authors: mendez mm.
Neurol Genet. 2020 Aug 4;6(5):e466. doi: 10.1212/NXG.0000000000000466. eCollection 2020 Oct.
Neurol Genet. 2020.
PMID: 32802951
Free PMC article.