An incidental finding in newborn screening leading to the diagnosis of a patient with ECHS1 mutations

Saved in:
Bibliographic Details
Published inMolecular genetics and metabolism reports Vol. 22; p. 100553
Main Authors Pajares, S, López, R M, Gort, L, Argudo-Ramírez, A, Marín, J L, González de Aledo-Castillo, J M, García-Villoria, J, Arranz, J A, Del Toro, M, Tort, F, Ugarteburu, O, Casellas, M D, Fernández, R, Ribes, A
Format Report
LanguageEnglish
Published 01.03.2020
Online AccessGet full text

Cover

More Information
Bibliography:ObjectType-Case Study-2
content type line 59
SourceType-Reports-1
ObjectType-Report-1
ISSN:2214-4269
2214-4269
DOI:10.1016/j.ymgmr.2019.100553