4 results on '"Kannan, Varun"'
Search Results
2. De novo mutations in GRIN1 cause extensive bilateral polymicrogyria
3. Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy
4. Arterial Spin Labeling Changes Parallel Asymmetric Perisylvian and Perirolandic Symptoms in 3 Pediatric Cases of Anti-NMDAR Encephalitis.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.