论文信息 - Clinical phenotype in X-linked Charcot-Marie-Tooth disease with an entire deletion of the connexin 32 coding sequence - 字舞流文

Clinical phenotype in X-linked Charcot-Marie-Tooth disease with an entire deletion of the connexin 32 coding sequence

K. Arimura | M. Nakagawa | H. Takashima | F. Miyashita | M. Osame | F. Umehara | W. Matsuyama | N. Takenouchi