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

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

DOI Full Paper Access

274

Citations

26

References

2004

Year

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

Nature Genetics

Mendelian DisorderBiochemistryGenetic DisorderNatural SciencesGeneticsInherited Metabolic DiseaseBiochemical GeneticsMolecular BiologyMolecular GeneticsDisease Gene IdentificationMedicineHartnup Disorder

References

	Year	Citations

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