Clinical characteristics of patients with spinocerebellar ataxias 1, 2, 3 and 6 in the US; a prospective observational study. Ashizawa, T., Figueroa, K. P, Perlman, S. L, Gomez, C. M, Wilmot, G. R, Schmahmann, J. D, Ying, S. H, Zesiewicz, T. A, Paulson, H. L, Shakkottai, V. G, Bushara, K. O, Kuo, S., Geschwind, M. D, Xia, G., Mazzoni, P., Krischer, J. P, Cuthbertson, D., Holbert, A. R., Ferguson, J. H, Pulst, S. M, & Subramony, S H Orphanet journal of rare diseases, 8:177, 2013.
Paper doi bibtex @article{pmid24225362,
author = {Ashizawa, Tetsuo and Figueroa, Karla P and Perlman, Susan L and Gomez, Christopher M and Wilmot, George R and Schmahmann, Jeremy D and Ying, Sarah H and Zesiewicz, Theresa A and Paulson, Henry L and Shakkottai, Vikram G and Bushara, Khalaf O and Kuo, Sheng-Han and Geschwind, Michael D and Xia, Guangbin and Mazzoni, Pietro and Krischer, Jeffrey P and Cuthbertson, David and Holbert, Amy Roberts and Ferguson, John H and Pulst, Stefan M and Subramony, S H},
title = {Clinical characteristics of patients with spinocerebellar ataxias 1, 2, 3 and 6 in the US; a prospective observational study},
journal = {Orphanet journal of rare diseases},
year = {2013},
volume = {8},
pages = {177},
doi = {10.1186/1750-1172-8-177},
url = {https://pubmed.ncbi.nlm.nih.gov/24225362/}
}
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