共 50 条
- [31] EIAV-Based Retinal Gene Therapy in the shaker1 Mouse Model for Usher Syndrome Type 1B: Development of UshStat PLOS ONE, 2014, 9 (04):
- [32] A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene Nature Genetics, 2000, 26 : 56 - 60
- [35] The Usher syndrome 1C protein harmonin regulates canonical Wnt signaling FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2023, 11
- [39] Usher syndrome type 1C - Localization to chromosome 11p14 and construction of a YAC contig DEGENERATIVE RETINAL DISEASES, 1997, : 303 - 312