|
 | Up a level |
Saleem, Quasar and Choudhry, Shweta and Mukerji, Mitali and Bashyam, Leena and Padma, Madakasira V and Chakravarthy, Ambar and Maheshwari, Mool Chand and Jain, Satish and Brahmachari, Samir K (2000) Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutation. In: Human Genetics, 106 (2). pp. 179-187.
