Delineating the neurological phenotype in children with defects in the ECHS1 or HIBCH gene
MartiâSanchez, L, BaideâMairena, H, MarcéâGrau, A, Pons, R, Skouma, A, LópezâLaso, E, Sigatullina, M, Rizzo, C, Semeraro, M, Martinelli, D, Carrozzo, R, DionisiâVici, C, GonzálezâGutiéJournal:
Journal of Inherited Metabolic Disease
DOI:
10.1002/jimd.12288
Date:
July, 2020
File:
PDF, 2.23 MB
2020
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