학술논문
Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients
Document Type
Artikel
Author
Carrozzo, R; Verrigni, D; Rasmussen, M; de Coo, R; Amartino, H; Bianchi, M; Buhas, D; Mesli, S; Naess, K; Born, AP; Woldseth, B; Prontera, P; Batbayli, M; Ravn, K; Joensen, F; Cordelli, DM; Santorelli, FM; Tulinius, M; Darin, N; Duno, M; Jouvencel, P; Burlina, A; Stangoni, G; Bertini, E; Redonnet-Vernhet, I; Wibrand, F; Dionisi-Vici, C; Uusimaa, J; Vieira, P; Osorio, AN; McFarland, R; Taylor, RW; Holme, E; Ostergaard, E
Source
Journal of inherited metabolic disease. 39(2):243-252
Subject
Language
English
English
English
ISSN
1573-2665