Hitoshi Sakuma

X‐Arrestin: a new retinal arrestin mapping to the X chromosome

Akira Murakami, Toshihiro Yajima, Hitoshi Sakuma et al. · FEBS Letters · 1993 · 120 citations

HRG4 (UNC119) mutation found in cone-rod dystrophy causes retinal degeneration in a transgenic model.

Akira Kobayashi, Tomomi Higashide, D.I. Hamasaki et al. · PubMed · 2000 · 119 citations

Point mutations of rhodopsin gene found in Japanese families with autosomal dominant retinitis pigmentosa (ADRP)

Keiko Fujiki, Yoshihiro Hotta, Mutsuko Hayakawa et al. · The Japanese Journal of Human Genetics · 1992 · 67 citations · Full text

Point Mutations, Genetic Disorder, Genetics +6

A Heterozygous Putative Null Mutation in ROM1 without a Mutation in Peripherin/RDS in a Family with Retinitis Pigmentosa

Hitoshi Sakuma, George Inana, Akira Murakami et al. · Genomics · 1995 · 35 citations · Full text

Biology, Protein Function, Molecular Physiology +15

Isolation and characterization of the human X-arrestin gene

Hitoshi Sakuma, Akira Murakami, Takuro Fujimaki et al. · Gene · 1998 · 28 citations · Full text