New aspects for the brain in Hartnup disease based on mining of high-resolution cellular mRNA expression data for SLC6A19

Hartnup disease is an autosomal recessive, metabolic disorder caused by mutations of the neutral amino acid transporter, SLC6A19/B0AT1. Reduced absorption in the intestine and kidney results in deficiencies in neutral amino acids and their down-stream metabolites, including niacin, associated with s...

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Bibliographic Details

Published in:	IBRO Neuroscience Reports
Main Authors:	Zachary Kravetz, Rainald Schmidt-Kastner
Format:	Article
Language:	English
Published:	Elsevier 2023-06-01
Subjects:	Hartnup disease Amino acid transporter Tryptophan SLC6A19 ACE2 Ependyma
Online Access:	http://www.sciencedirect.com/science/article/pii/S2667242123000271