Trisomy 17p associated with Charcot-Marie-Tooth neuropathy type 1A phenotype: evidence for gene dosage as a mechanism in CMT1A.
All Authors:
Authors
Chance PF, Bird TD, Matsunami N, Lensch MW, Brothman AR, Feldman GM.
Author Profiles:
Persons
Publish Date:
Date
Journal:
Venue / Journal
Neurology
Additional Journal Information
42(12):2295-9