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Browsing by Author Ng, Cynthia

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01 Broer et al Iminoglycinuria and hyperglycinuria 2008.pdf.jpg

Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters

Author(s)Bröer, Stefan; Bailey, Charles G.; Kowalczuk, Sonja, et al
TypeJournal article
Date Published2008
Date Created-
01_Bailey_Loss-of-function_mutations_in_2011.pdf.jpg

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
TypeJournal article
Date Published2011
Date Created-
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