Hunter disease eClinic: interactive, computer-assisted, problem-based approach to independent learning about a rare genetic disease

por Al-Jasmi, Fatma, Moldovan, Laura, Clarke, Joe TR
Publicado 2010

Methylmalonyl-coA epimerase deficiency: A new case, with an acute metabolic presentation and an intronic splicing mutation in the MCEE gene

por Waters, Paula J., Thuriot, Fanny, Clarke, Joe T.R., Gravel, Serge, Watkins, David, Rosenblatt, David S., Lévesque, Sébastien
Publicado 2016