Showing results 1 to 5 of 5
Title | Author(s) | Issue Date | Views | |
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2010 | 187 | |||
A Missense Mutation in SLC33A1, which Encodes the Acetyl-CoA Transporter, Causes Autosomal-Dominant Spastic Paraplegia (SPG42) Journal:American Journal of Human Genetics | 2008 | 166 | ||
2020 | 26 | |||
2010 | 283 | |||
2012 | 57 |