Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene
Year: 2001
Type: article
Study design: Observational Study
Source: Nature Genetics
DOI: 10.1038/ng1001-184
Authors: Hidetoshi Date, Osamu Onodera, Hajime Tanaka, Kiyoshi Iwabuchi, Kazutoshi Uekawa, Shuichi Igarashi, Ryoko Koike, Tadashi Hiroi, Tatsuhiko Yuasa, Yutaka Awaya, Tetsuo Sakai, Tatsuya Takahashi, Hideki Nagatomo, Yoshiki Sekijima, Izumi Kawachi, Yoshihisa Takiyama, Masatoyo Nishizawa, Nobuyoshi Fukuhara, Kayoko Saito, Sumio Sugano, Shoji Tsuji
Institutions: Brain Research Institute, Niigata University, Niigata University, Kanagawa Rehabilitation Hospital, National Center of Neurology and Psychiatry, Kohnodai Hospital, National Center for Global Health and Medicine, Yokohama City University Medical Center, Yokohama City University, Shinshu University, Jichi Medical University, Jichi Medical University Hospital, International University of Health and Welfare, Saigata National Hospital, Tokyo Women's Medical University, Institute of Medical Science, The University of Tokyo, The University of Tokyo
Language: English
Subfield: Cellular and Molecular Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: closed
OpenAlex ID: W1536477417