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Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutation

✍ Scribed by Q. Saleem; S. Choudhry; M. Mukerji; L. Bashyam; M.V. Padma; A. Chakravarthy; M.C. Maheshwari; S. Jain; S.K. Brahmachari


Publisher
Springer
Year
2000
Tongue
English
Weight
117 KB
Volume
106
Category
Article
ISSN
0340-6717

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