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Hartnup disorder: Polymorphisms identified in the neutral amino acid transporter SLC1A5

  • Published:2002-11 Issue:6 Volume:25 Page:437-448
  • ISSN:0141-8955
  • Container-title:Journal of Inherited Metabolic Disease
  • language:en
  • Short-container-title:J Inherit Metab Dis

Author:

Potter S. J.1,Lu A.1,Wilcken B.2,Green K.2,Rasko J. E. J.134

Affiliation:

1. ; Centenary Institute of Cancer Medicine and Cell Biology; Gene Therapy Research Unit Australia

2. ; New South Wales Biochemical Genetics Service; The Children's Hospital at Westmead; Australia

3. ; Sydney Cancer Centre; Royal Prince Alfred Hospital; NSW Australia

4. ; Gene Therapy Research Unit; Centenary Institute; Locked Bag No. 6 Newtown NSW 2042 Australia

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Cited by 17 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. How Much Do You Fuse? A Comparison of Cell Fusion Assays in a Breast Cancer Model;International Journal of Molecular Sciences;2024-05-23

2. Amino Acid Transport Defects;Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases;2022

3. Accurate discrimination of Hartnup disorder from other aminoacidurias using a diagnostic ratio;Molecular Genetics and Metabolism Reports;2020-03

4. De la disrupción en el metabolismo del triptófano a la complejidad clínica de la enfermedad de Hartnup;Medicina e Investigación;2014-07

5. Epigenetic and non-epigenetic regulation of syncytin-1 expression in human placenta and cancer tissues;Cellular Signalling;2014-03
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