Items where Author is "Mittal, Uma"

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | No Grouping
Number of items: 6.

Krishna, Nithin ; Mohan, Surendra ; Yashavantha, B. S. ; Rammurthy, A. ; Kiran Kumar, H. B. ; Mittal, Uma ; Tyagi, Shivani ; Mukerji, Mitali ; Jain, Sanjeev ; Pal, Pramod Kumar ; Purushottam, Meera (2007) SCA 1, SCA 2 & SCA 3/MJD mutations in ataxia syndromes in Southern India Indian Journal of Medical Research, 126 (5). pp. 465-470. ISSN 0971-5916

Mittal, Uma ; Srivastava, Achal K. ; Jain, Satish ; Jain, Sanjeev ; Mukerji, Mitali (2005) Founder haplotype for Machado-Joseph disease in the Indian population Archives of Neurology, 62 (4). pp. 637-640. ISSN 0003-9942

Mittal, Uma ; Sharma, Sangeeta ; Chopra, Rupali ; Dheeraj, Kalladka ; Pal, Pramod Kr. ; Srivastava, Achal K. ; Mukerji, Mitali (2005) Insights into the mutational history and prevalence of SCA1 in the Indian population through anchored polymorphisms Human Genetics, 118 (1). Article ID 107. ISSN 0340-6717

Mittal, Uma ; Roy, Sanghamitra ; Jain, Satish ; Srivastava, Achal K. ; Mukerji, Mitali (2005) Post-zygotic de novo trinucleotide repeat expansion at spinocerebellar ataxia type 7 locus: evidence from an Indian family Journal of Human Genetics, 50 (3). pp. 155-157. ISSN 1434-5161

Ragothaman, Mona ; Sarangmath, Nagaraja ; Chaudhary, Shashi ; Khare, Vishwamohini ; Mittal, Uma ; Sharma, Sangeeta ; Komatireddy, Sreelatha ; Chakrabarti, Subhabrata ; Mukerji, Mitali ; Juyal, Ramesh C. ; Thelma, B. K. ; Muthane, Uday B. (2004) Complex phenotypes in an Indian family with homozygous SCA2 mutations Annals of Neurology, 55 (1). pp. 130-133. ISSN 0364-5134

Pandey, Neeraj ; Mittal, Uma ; Srivastava, Achal K. ; Mukerji, Mitali (2004) SMARCA2 and THAP11: potential candidates for polyglutamine disorders as evidenced from polymorphism and protein-folding simulation studies Journal of Human Genetics, 49 (11). pp. 596-602. ISSN 1434-5161

This list was generated on Fri Sep 27 13:02:53 2024 UTC.