R. Walsh

Clinical , biochemical , and genetic features of four patients with short-chain enoyl-CoA hydratase ( ECHS 1 ) deficiency

Reilly, Robert W. Taylor, S. Ferdinandusse, 2018 .

Clinical, biochemical, and genetic features of four patients with short‐chain enoyl‐CoA hydratase (ECHS1) deficiency

Robert W. Taylor, S. Ferdinandusse, H. Waterham, 2018, American journal of medical genetics. Part A.

Mitochondrial cytopathies, phenotypic heterogeneity and a high incidence.

G. Brown, P. Rustin, M. King, 2006, Irish medical journal.

What is the origin of 3-methylglutaconic acid?

R. Walsh, P. Mayne, G. Roche, 1999, Journal of Inherited Metabolic Disease.

3-methylglutaconic aciduria in pregnancy

E. Naughten, R. Walsh, P. Mayne, 1997, The Lancet.