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| Abbas MM, Govindappa ST, Sudhaman S, et al. (2016) Early Onset Parkinson's disease due to DJ1 mutations: An Indian study. Parkinsonism & Related Disorders |
| Sudhaman S, Prasad K, Behari M, et al. (2016) Discovery of a frameshift mutation in podocalyxin-like (PODXL) gene, coding for a neural adhesion molecule, as causal for autosomal-recessive juvenile Parkinsonism. Journal of Medical Genetics. 53: 450-6 |
| Geetha TS, Michealraj KA, Kabra M, et al. (2014) Targeted deep resequencing identifies MID2 mutation for X-linked intellectual disability with varied disease severity in a large kindred from India. Human Mutation. 35: 41-4 |
| Sudhaman S, Behari M, Govindappa ST, et al. (2013) VPS35 and EIF4G1 mutations are rare in Parkinson's disease among Indians. Neurobiology of Aging. 34: 2442.e1-3 |
| Mittal K, Kabra M, Juyal R, et al. (2011) De novo deletion in MECP2 in a monozygotic twin pair: a case report. Bmc Medical Genetics. 12: 113 |
| Mittal K, Gupta N, Kabra M, et al. (2011) Distinct de novo deletions in a brother-sister pair with RTT: a case report. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 859-63 |
| Ragothaman M, Sarangmath N, Chaudhary S, et al. (2004) Complex phenotypes in an Indian family with homozygous SCA2 mutations. Annals of Neurology. 55: 130-3 |