A Superti-Furga

Point mutations throughout the GLI3 gene cause Greig cephalopolysyndactyly syndrome.

R Rizzo, J Kunze, M. Kalff-Suske, 1999, Human molecular genetics.

Clinical course, early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiency.

W Lehnert, M. Durán, E. Christensen, 1996, Neuropediatrics.