(Q73621643)
Statements
Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutation (English)
Q Saleem
S Choudhry
M Mukerji
L Bashyam
M V Padma
A Chakravarthy
M C Maheshwari
S Jain
S K Brahmachari
1 February 2000