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Merinero B, Perez B, Perez-Cerda C, Rincon A, Desviat LR, Martinez MA, Sala PR, Garcia MJ, Aldamiz-Echevarria L, Campos J, Cornejo V, Del Toro M, Mahfoud A, Martnez-Pardo M, Parini R, Pedrn C, Pea-Quintana L, Prez M, Pourfarzam M, Ugarte M: Methylmalonic acidaemia: examination of genotype and biochemical data in 32 patients belonging to mut, cblA or cblB complementation group
10.1371/journal.pone.0092842 [DOI] [PMC free article] [PubMed] [Google Scholar] 55.Cuturic M, Abramson RK, Moran RR, Hardin JW, Hall AV
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A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency
