Trisomy 17p associated with Charcot-Marie-Tooth neuropathy type 1A phenotype: evidence for gene dosage as a mechanism in CMT1A.

Persons

Willy Lensch

Venue / Journal

Neurology

Date

Tue, 12/01/1992 - 12:00

Additional Journal Information

42(12):2295-9

Authors

Chance PF, Bird TD, Matsunami N, Lensch MW, Brothman AR, Feldman GM.

Pubmed URL

http://www.ncbi.nlm.nih.gov/pubmed/1461382