Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters

Stefan Bröer, Charles G. Bailey, Sonja Kowalczuk, Cynthia Ng, Jessica M. Vanslambrouck, Helen Rodgers, Christiane Auray-Blais, Juleen A. Cavanaugh, Angelika Bröer, John E.J. Rasko

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

    97 Citations (Scopus)

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    Biochemistry, Genetics and Molecular Biology