Takenori Endo

Adhalin gene mutations in patients with autosomal recessive childhood onset muscular dystrophy with adhalin deficiency.

H Kawai, M. Akaike, Takenori Endo et al. · Journal of Clinical Investigation · 1995 · 43 citations · Full text

Rare Diseases, Adhalin Gene Mutations, Developmental Biology +12

Functional association between nicotinic acetylcholine receptor and sarcomeric proteins via actin and desmin filaments

Takao Mitsui, Masakazu Kawajiri, Makoto Kunishige et al. · Journal of Cellular Biochemistry · 2000 · 33 citations

Muscle Function, Myosin Mg, Cytoskeleton +17

New missense mutation in the alpha-sarcoglycan gene in a Japanese patient with severe childhood autosomal recessive muscular dystrophy with incomplete alpha-sarcoglycan deficiency

Itsuro Higuchi, Hiroyuki Iwaki, Hisaomi Kawai et al. · Journal of the Neurological Sciences · 1997 · 10 citations

Rare Diseases, Mendelian Disorder, Genetic Disorder +9