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Molecular Cloning of Mouse Amino Acid Transport System B0, a Neutral Amino Acid Transporter Related to Hartnup Disorder

✍ Scribed by Broer, A.; Klingel, K.; Kowalczuk, S.; Rasko, J. E. J.; Cavanaugh, J.; Broer, S.

Book ID
118261046
Publisher
The American Society for Biochemistry and Molecular Biology
Year
2004
Tongue
English
Weight
764 KB
Volume
279
Category
Article
ISSN
0021-9258

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## Abstract Hartnup disorder (OMIM 234500) is an autosomal recessive disorder, which was first described in 1956 as an aminoaciduria of neutral amino acids accompanied by a variety of symptoms, such as a photo‐sensitive skin‐rash and cerebellar ataxia. The disorder is caused by mutations in the neu