Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19

Heng F. Seow, Stefan Bröer, Angelika Bröer, Charles G. Bailey, Simon J. Potter, Juleen A. Cavanaugh, John E.J. Rasko*

*Corresponding author for this work

    Research output: Contribution to journal › Article › peer-review

    245 Citations (Scopus)

    Fingerprint

    Dive into the research topics of 'Hartnup disorder is caused by mutations in the gene encoding the neutral amino acid transporter SLC6A19'. Together they form a unique fingerprint.
    Sort by

    Pharmacology, Toxicology and Pharmaceutical Science

    Biochemistry, Genetics and Molecular Biology

    Neuroscience

    Nursing and Health Professions