共 50 条
- [45] FATAL FAMILIAL INSOMNIA (FFI) - A PRION DISEASE WITH A MUTATION AT CODON-178 OF THE PRION PROTEIN GENE [J]. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1992, 51 (03): : 353 - 353
- [48] DISTINCT NEUROPSYCHOLOGICAL PROFILES CORRESPOND TO DISTRIBUTION OF CORTICAL THINNING IN INHERITED PRION DISEASE CAUSED BY INSERTIONAL MUTATION [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2010, 81 (11): : E42 - E43
- [49] Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation [J]. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2012, 83 (01): : 109 - 114
- [50] FLAGELLAR ABNORMALITIES IN SPERM OF A TRANSGENIC MOUSE INSERTIONAL MUTANT [J]. ANATOMICAL RECORD, 1987, 218 (01): : A52 - A52