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Publications (22)
- Detection of Common Deletion Mutations (– α3.7 and – α4.2 kb) in HBA gene and Genotype-Phenotype Correlation Save
- Clarification on "Myotonic Dystrophy Type 1 - An Atypical Presentation". Save
- Association of dopamine receptor D3 polymorphism with Levodopa-induced Dyskinesia: A study on Parkinson's disease patients from India. Save
- Secondary prevention with a structured semi-interactive stroke prevention package in INDIA (SPRINT INDIA): a multicentre, randomised controlled trial. Save
- Genetic Polymorphisms in DRD4 and Risk for Parkinson's Disease Among Eastern Indians. Save
- Identification of GBA mutations among neurodegenerative disease patients from eastern India. Save
- Mitochondrial DNA Haplogroups and Three Independent Polymorphisms have no Association with the Risk of Parkinson's Disease in East Indian Population. Save
- Role of LRRK2 variant p.Gly2019Ser in patients with Parkinsonism. Save
- Primary generalized dystonia due to TOR1A ΔGAG mutation in an Indian family with intrafamilial clinical heterogeneity. Save
- Dopamine β Hydroxylase (DBH) is a potential modifier gene associated with Parkinson's disease in Eastern India. Save