Genome-wide association study identifies ZFHX1B as a susceptibility locus for severe myopia
Year: 2013
Type: review
Study design: Observational Study
Source: Human Molecular Genetics
DOI: 10.1093/hmg/ddt385
Authors: Chiea Chuen Khor, Masahiro Miyake, Li Jia Chen, Yi Shi, Veluchamy A. Barathi, Fan Qiao, Isao Nakata, Kenji Yamashiro, Xin Zhou, Pancy O.S. Tam, Ching-Yu Cheng, E Shyong Tai, Eranga N. Vithana, Tin Aung, Yik-Ying Teo, Tien-Yin Wong, Muka Moriyama, Kyoko Ohno-Matsui, Manabu Mochizuki, Fumihiko Matsuda, Nagahama Study Group, Rita Y.Y. Yong, Eric P.H. Yap, Zhenglin Yang, Chi Pui Pang, Seang-Mei Saw, Nagahisa Yoshimura
Institutions: Singapore Eye Research Institute, Genome Institute of Singapore, Kyoto University, Center for Genomic Medicine, Graduate School of Medicine, Kyoto University, Chinese University of Hong Kong, Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital, National University of Singapore, Duke-NUS Medical School, Tokyo Medical and Dental University, DSO National Laboratories
Language: English
Subfield: Epidemiology
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W2159793244