Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Ji-Feng Wan"'
Autor:
Ping Hou, Ji-Feng Wan, Yan-Shan Liu, Jian-Huan Chen, En-Min Li, Qian-Hao Yao, Jia-Qi Pan, Shao-Qiang Liu, Jia-Li Zhang, Ruo-Nan Gao, Zhou-Heng Xu, Ji-Hong Wang, Jun-Hua Rao, Xu-Bin Pan, Chun-Yan Ren
Publikováno v:
Biochemical and Biophysical Research Communications. 531:172-179
Mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene, are the major cause of X-linked retinitis pigmentosa (RP), in which exon open reading frame 15 (ORF15) of RPGR has been implicated to play a substantial role. We identified a novel h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a75c063039bf48d99a73eacbaab06453
https://doi.org/10.1016/j.bbrc.2020.06.109
https://doi.org/10.1016/j.bbrc.2020.06.109
Autor:
Zhou-Heng Xu, Ji-Hong Wang, Ji-Feng Wan, Ping Hou, Jia-Li Zhang, Chun-Yan Ren, Shao-Qiang Liu, Jia-Qi Pan, Xu-Bin Pan, Jian-Huan Chen, Nuo-Nan Gao, Yan-Shan Liu, En-Min Li, Jun-Hua Rao, Qian-Hao Yao
Mutations in the retinitis pigmentosa GTPase regulator (RPGR) gene, are the major cause of X-linked retinitis pigmentosa (RP). Herein we used whole-exome sequencing to screen possible novel RPGR mutations in RP patients, and identified a novel missen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b06e4c6499abcb58c384112348d1801
https://doi.org/10.1101/2020.05.22.109884
https://doi.org/10.1101/2020.05.22.109884
