(Q71690188)
Statements
[A familial Charcot-Marie-Tooth disease type 1B (CMTD1B) manifesting a new mutation of myelin P0 gene] (English)
Mitsui Y
Matsui T
Nakamura Y
Takahashi M
Yoshikawa H
1 November 1994
scientific article published on 01 November 1994