Allan M Lund

Genetic disease is a common cause of bilateral childhood cataract in Denmark

K. Grønskov, L. Roos, L. Kessel, 2021, Ophthalmic genetics.

No effect of triheptanoin in patients with phosphofructokinase deficiency

P. Laforêt, J. Vissing, G. van Hall, 2022, Neuromuscular Disorders.

Update of the pompe disease mutation database with 60 novel GAA sequence variants and additional studies on the functional effect of 34 previously reported variants

S. Marie, W. Robberecht, B. Engelen, 2012, Human mutation.

Mucopolysaccharidoses in the Scandinavian countries: incidence and prevalence

J. Månsson, G. Malm, A. Heiberg, 2008, Acta paediatrica.