Entries of Nilwarangkoon, Sirinun on the publication server
 | Up a level |
Jump to: 2004
Number of items: 1.
2004
Kleta, Robert, Romeo, Elisa, Ristic, Zorica, Ohura, Toshihiro, Stuart, Caroline, Arcos-Burgos, Mauricio 
, Dave, Mital H, Wagner, Carsten A, Camargo, Simone R M , Inoue, Sumiko, Matsuura, Norio, Helip-Wooley, Amanda, Bockenhauer, Detlef , Warth, Richard , Bernardini, Isa, Visser, Gepke, Eggermann, Thomas, Lee, Philip, Chairoungdua, Arthit, Jutabha, Promsuk, Babu, Ellappan, Nilwarangkoon, Sirinun, Anzai, Naohiko, Kanai, Yoshikatsu, Verrey, Francois , Gahl, William A and Koizumi, Akio
(2004)
Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder.
Nature Genetics 36 (9), pp. 999-1002.
Fulltext not available.
, Dave, Mital H, Wagner, Carsten A, Camargo, Simone R M , Inoue, Sumiko, Matsuura, Norio, Helip-Wooley, Amanda, Bockenhauer, Detlef , Warth, Richard , Bernardini, Isa, Visser, Gepke, Eggermann, Thomas, Lee, Philip, Chairoungdua, Arthit, Jutabha, Promsuk, Babu, Ellappan, Nilwarangkoon, Sirinun, Anzai, Naohiko, Kanai, Yoshikatsu, Verrey, Francois , Gahl, William A and Koizumi, Akio
(2004)
Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder.
Nature Genetics 36 (9), pp. 999-1002.
Fulltext not available.