Browsing by Author Ryan, Renae M.
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Loss-of-function mutations in the glutamate transporter SLC1A1 cause human dicarboxylic aminoaciduria
Author(s) | Bailey, Charles G.; Ryan, Renae M.; Thoeng, Annora D., et al |
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Type | Journal article |
Date Published | 2011 |
Date Created | - |
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