Work

A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55)

Year: 2012

Type: article

Source: Journal of Medical Genetics

DOI: 10.1136/jmedgenet-2012-101212

Authors: Haruo Shimazaki, Yoshihisa Takiyama, Hiroyuki Ishiura, Chika Sakai, Yuichi Matsushima, Hideyuki Hatakeyama, Junko Honda, Kumi Sakoe, Tametou Naoi, Michito Namekawa, Yoko Fukuda, Yuji Takahashi, Jun Goto, Shoji Tsuji, Yu-ichi Goto, Imaharu Nakano

Institutions: Jichi Medical University, Jichi Medical University Hospital, University of Yamanashi, The University of Tokyo, National Center of Neurology and Psychiatry, National Institute of Neuroscience

Language: English

Topic: Hereditary Neurological Disorders

Subfield: Cellular and Molecular Neuroscience

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funder: Japan Society for the Promotion of Science

Award: Identification of the novel genes responsible for hereditary spastic paraplegias

OpenAlex ID: W2113687948

FWCI: 3.752

Cites: 39

Cited by: 87

Related to: 10