Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

A point mutation associated with a severe phenotype of neurofibromatosis 2.

MacCollin M, Braverman N, Viskochil D, Ruttledge M, Davis K, Ojemann R, Gusella J, Parry DM. A point mutation associated with a severe phenotype of neurofibromatosis 2. Ann Neurol. 1996 Sep; 40(3):440-5.

View in: PubMed

Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.