A mouse model of type B cystinuria due to spontaneous mutation in FVB/NJcl mice
A mouse model of type B cystinuria due to spontaneous mutation in FVB/NJcl mice
About this item
Full title
Author / Creator
Publisher
Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title
Language
English
Formats
Publication information
Publisher
Berlin/Heidelberg: Springer Berlin Heidelberg
Subjects
More information
Scope and Contents
Contents
Cystinuria is an autosomal metabolic disorder caused by mutations in the
SLC3A1
and
SLC7A9
genes, encoding the amino acid transporter proteins rBAT and b
0,+
AT, respectively. Based on the causative gene, cystinuria is classified into 3 types: type A (
SLC3A1
), type B (
SLC7A9
), and type AB (
SLC3A1
and
SLC7...
Alternative Titles
Full title
A mouse model of type B cystinuria due to spontaneous mutation in FVB/NJcl mice
Authors, Artists and Contributors
Author / Creator
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Primary Identifiers
Record Identifier
TN_cdi_proquest_journals_2726605022
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2726605022
Other Identifiers
ISSN
2194-7228
E-ISSN
2194-7236
DOI
10.1007/s00240-022-01356-9
