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Complex phenotypes in an Indian family with homozygous SCA2 mutations.
Ragothaman M, Sarangmath N, Chaudhary S, Khare V, Mittal U, Sharma S, Komatireddy S, Chakrabarti S, Mukerji M, Juyal RC, Thelma BK, Muthane UB. Ragothaman M, et al. Among authors: thelma bk. Ann Neurol. 2004 Jan;55(1):130-3. doi: 10.1002/ana.10815. Ann Neurol. 2004. PMID: 14705123
Parkin mutations in familial and sporadic Parkinson's disease among Indians.
Chaudhary S, Behari M, Dihana M, Swaminath PV, Govindappa ST, Jayaram S, Goyal V, Maitra A, Muthane UB, Juyal RC, Thelma BK. Chaudhary S, et al. Among authors: thelma bk. Parkinsonism Relat Disord. 2006 May;12(4):239-45. doi: 10.1016/j.parkreldis.2005.12.004. Epub 2006 Feb 24. Parkinsonism Relat Disord. 2006. PMID: 16500134
Genetic susceptibility to Parkinson's disease among South and North Indians: I. Role of polymorphisms in dopamine receptor and transporter genes and association of DRD4 120-bp duplication marker.
Juyal RC, Das M, Punia S, Behari M, Nainwal G, Singh S, Swaminath PV, Govindappa ST, Jayaram S, Muthane UB, Thelma BK. Juyal RC, et al. Among authors: thelma bk. Neurogenetics. 2006 Nov;7(4):223-9. doi: 10.1007/s10048-006-0048-y. Epub 2006 Jul 1. Neurogenetics. 2006. PMID: 16816977
138 results