-
Bröer, S, Bailey, CG, Kowalczuk, S, Ng, C, Vanslambrouck, JM, Rodgers, H, Auray-Blais, C, Cavanaugh, JA, Bröer, A, Rasko, JEJ.
Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters..
J Clin Invest
118(12)
:
3881 -3892
2008
view publication
-
Kowalczuk, S, Bröer, A, Tietze, N, Vanslambrouck, JM, Rasko, JEJ, Bröer, S.
A protein complex in the brush-border membrane explains a Hartnup disorder allele..
FASEB J
22(8)
:
2880 -2887
2008
view publication
-
Gardiner, J, Barton, D, Vanslambrouck, JM, Braet, F, Hall, D, Marc, J, Overall, R.
Defects in tongue papillae and taste sensation indicate a problem with neurotrophic support in various neurological diseases..
Neuroscientist
14(3)
:
240 -250
2008
view publication