@article{oai:repo.qst.go.jp:00043913,
 author = {Seki, Naohiko and Muramatsu, Masa-aki and Sugano, Sumio and Suzuki, Yutaka and Nakagawara, Akira and Hayashi, Akiko and Hori, Tadaaki and Saito, Toshiyuki and 関 直彦 and 林 昭子 and 堀 雅明 and 齋藤 俊行},
 journal = {Journal of Human Genetics},
 month = {},
 note = {Huntington disease (HD) is an inherited neurodegenerative disorder which is associated with CAG expansion in the coding region of the gene for huntingtin protein. Recently, a huntingtin interacting protein, HIP1, was isolated by the yeast two-hybrid system. Here we report the isolation of a cDNA clone for HIP1R (huntingtin interacting protein-1 related), which encodes a predicted protein product sharing a striking homology with HIP1. RT-PCR analysis showed that the messenger RNA was ubiquitously expressed in various human tissues. Based on PCR-assisted analysis of a radiation hybrid panel and fluorescence in situ hybridization, HIP1R was localized to the q24 region of chromosome 12.},
 pages = {268--271},
 title = {Cloning, expression analysis, and chromosomal localization of HIP1R, an isolog of huntingtin interacting protein (HIP1).},
 volume = {43},
 year = {1998}
}