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  2. Details for: Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder.
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Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder. [electronic resource]

By:
  • Kleta, Robert
Contributor(s):
  • 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
  • Koizumi, Akio
Producer: 20041004Description: 999-1002 p. digitalISSN:
  • 1061-4036
Subject(s):
  • Amino Acid Sequence
  • Amino Acid Transport Systems, Neutral -- genetics
  • Animals
  • Base Sequence
  • Chromosome Mapping
  • Hartnup Disease -- genetics
  • Humans
  • Kidney -- metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Molecular Sequence Data
  • Mutation
  • Pedigree
Online resources:
  • Available from publisher's website
In: Nature genetics vol. 36
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't

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Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder.

APA

Kleta R., Romeo E., Ristic Z., Ohura T., Stuart C., Arcos-Burgos M., Dave M. H., Wagner C. A., Camargo S. R. M., Inoue S., Matsuura N., Helip-Wooley A., Bockenhauer D., Warth R., Bernardini I., Visser G., Eggermann T., Lee P., Chairoungdua A., Jutabha P., Babu E., Nilwarangkoon S., Anzai N., Kanai Y., Verrey F., Gahl W. A. & Koizumi A. (20041004). Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder. : Nature genetics.

Chicago

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. 20041004. Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder. : Nature genetics.

Harvard

Kleta R., Romeo E., Ristic Z., Ohura T., Stuart C., Arcos-Burgos M., Dave M. H., Wagner C. A., Camargo S. R. M., Inoue S., Matsuura N., Helip-Wooley A., Bockenhauer D., Warth R., Bernardini I., Visser G., Eggermann T., Lee P., Chairoungdua A., Jutabha P., Babu E., Nilwarangkoon S., Anzai N., Kanai Y., Verrey F., Gahl W. A. and Koizumi A. (20041004). Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder. : Nature genetics.

MLA

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. Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder. : Nature genetics. 20041004.

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