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Browsing by Author Kowalczuk, Sonja

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Showing results 3 to 7 of 7

Further Evidence for Allelic Heterogeneity in Hartnup Disorder

Author(s)Azmanov, Dimitar; Kowalczuk, Sonja; Rodgers, Helen, et al
TypeJournal article
Date Published2008
Date Created-
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-

Molecular Cloning of Mouse Amino Acid Transport System B 0 , a Neutral Amino Acid Transporter Related to Hartnup Disorder

Author(s)Broer, Angelika; Klingel, Karen; Kowalczuk, Sonja, et al
TypeJournal article
Date Published2004
Date Created-

Molecular cloning of the mouse IMINO system: an Na+- and CI--dependent proline transporter

Author(s)Kowalczuk, Sonja; Broer, Angelika; Kingsland (previously Munzinger), Michael, et al
TypeJournal article
Date Published2005
Date Created-

The orphan transporter v7-3 (slc6a15) is a Na + -dependent neutral amino acid transporter (B 0 AT2)

Author(s)Broer, Angelika; Tietze, Nadine; Kowalczuk, Sonja, et al
TypeJournal article
Date Published2006
Date Created-

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