Identification of new mutations in the Cu/Zn superoxide dismutase gene of patients with familial amyotrophic lateral sclerosis.

nork Pramatarova, A, Figlewicz, D A, Krizus, A, Han, F Y, Ceballos-Picot, I, Nicole, A, Dib, M, Meininger, V, Brown, R H, Rouleau, G A
Argitaratua 1995

Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease.

nork Ruttledge, M. H., Andermann, A. A., Phelan, C. M., Claudio, J. O., Han, F. Y., Chretien, N., Rangaratnam, S., MacCollin, M., Short, P., Parry, D., Michels, V., Riccardi, V. M., Weksberg, R., Kitamura, K., Bradburn, J. M., Hall, B. D., Propping, P., Rouleau, G. A.
Argitaratua 1996