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Mitochondrial diseases in North America: An analysis of the NAMDC Registry

Barca, E; Long, YL; Cooley, V; Schoenaker, R; Emmanuele, V; DiMauro, S; Cohen, BH; Karaa, A; Vladutiu, GD; Haas, R; Van Hove, JLK; Scaglia, F; Parikh, S; Bedoyan, JK; DeBrosse, SD; Gavrilova, RH; Saneto, RP; Enns, GM; Stacpoole, PW; Ganesh, J; Larson, A; Zolkipli-Cunningham, Z; Falk, MJ; Goldstein, AC; Tarnopolsky, M; Gropman, A; Camp, K; Krotoski, D; Engelstad, K; Rosales, XQ; Kriger, J; Grier, J; Buchsbaum, R; Thompson, JLP; Hirano, M

Hirano, M (corresponding author), Columbia Univ, Dept Neurol, Med Ctr, New York, NY 10032 USA.

NEUROLOGY-GENETICS, 2020; 6 (2):

Abstract

ObjectiveTo describe clinical, biochemical, and genetic features of participants with mitochondrial diseases (MtDs) enrolled in the North American Mit......

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