Patitucci, Alessandra

Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

Züchner, S., Mersiyanova, I. V., Muglia, M., Bissar-Tadmouri, N., Rochelle, J., Dadali, E. L., Zappia, M., Nelis, E., Patitucci, A., Senderek, J., et al. (2004) · Nature Genetics

Hereditary Neurological DisordersMitochondrial Function and Pathology

Cited by 1,572

A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL

Mazzei, R., Conforti, F. L., Lanza, P. L., Sprovieri, T., Lupo, M. R., Gallo, O., Patitucci, A., Magariello, A., Caracciolo, M., Gabriele, A. L., et al. (2004) · Neurology

Cerebrovascular and genetic disordersGenetic Neurodegenerative Diseases

Cited by 48