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Results 1 - 1 of 1 for Neutral 1 amino acid transport defect
  1. SLC6A19 gene 
    ... the SLC6A19 gene have been found to cause Hartnup disease. This condition is characterized by increased levels of ... cognitive problems. Most of the mutations that cause Hartnup disease change single amino acids in the B0AT1 protein, ...
    https://medlineplus.gov/genetics/gene/slc6a19 - Genetics