Tohru Ikegami

Molecular analysis in Japanese patients with Charcot-Marie-Tooth disease: DGGE analysis for PMP22, MPZ, and Cx32/GJB1 mutations

Chikahiko Numakura, Changqing Lin, Tohru Ikegami et al. · Human Mutation · 2002 · 64 citations

Life Sciences, Genetics, Molecular Genetics +14

A Novel Homozygous Mutation of the Myelin Po Gene Producing Dejerine–Sottas Disease (Hereditary Motor and Sensory Neuropathy Type III)

Tohru Ikegami, Garth A. Nicholson, Hiroyuki Ikeda et al. · Biochemical and Biophysical Research Communications · 1996 · 49 citations

Medicine, Genetics, Neurology +14

Locations of crossover breakpoints within the CMT1A-REP repeat in Japanese patients with CMT1A and HNPP

Masahiko Yamamoto, Takeshi Yasuda, Kiyoshi Hayasaka et al. · Human Genetics · 1997 · 26 citations

Life Sciences, Genetics, Molecular Genetics +6

Novel mutations of the peripheral myelin protein22 gene in two pedigrees with Dejerine-Sottas disease

Tohru Ikegami, Hiroyuki Ikeda, Masahiro Aoyama et al. · Human Genetics · 1998 · 25 citations

Medicine, Genetics, Molecular Genetics +16

Deletion and Nonsense Mutations of the Connexin 32 Gene Associated with Charcot-Marie-Tooth Disease.

Changqing Lin, Chikahiko Numakura, Tohru Ikegami et al. · The Tohoku Journal of Experimental Medicine · 1999 · 23 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11