The Genomic Region Encompassing the Nephropathic Cystinosis Gene (CTNS): Complete Sequencing of a 200-kb Segment and Discovery of a Novel Gene within the Common Cystinosis-Causing Deletion

Nephropathic cystinosis is an autosomal recessive disorder caused by the defective transport of cystine out of lysosomes. Recently, the causative gene (CTNS) was identified and presumed to encode an integral membrane protein called cystinosin. Many of the disease-associated mutations in CTNS are del...

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Pubblicato in:	Genome Res
Autori principali:	Touchman, Jeffrey W., Anikster, Yair, Dietrich, Nicole L., Maduro, Valerie V. Braden, McDowell, Geraldine, Shotelersuk, Vorasuk, Bouffard, Gerard G., Beckstrom-Sternberg, Stephen M., Gahl, William A., Green, Eric D.
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	Cold Spring Harbor Laboratory Press 2000
Soggetti:	Report
Accesso online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC310836/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10673275/ https://ncbi.nlm.nih.govhttps://doi.org/10.1101/gr.10.2.165
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