Genetic basis of cystinosis in Tunisian patients: Identification of novel mutation in CTNS gene

Nephropathic cystinosis (NC) is an autosomal recessive disorder characterized by defective transport of cystine across the lysosomal membrane and resulting in renal, ophthalmic, and other organ abnormalities. Mutations in the CTNS gene cause a deficiency of the transport protein, cystinosin. This st...

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Detalles Bibliográficos
Autores principales: Chkioua, Latifa, Khedhiri, Souhir, Grissa, Oussama, Aloui, Chaker, Turkia, Hadhami Ben, Ferchichi, Salima, Miled, Abdelhedi, Froissart, Roseline, Acquaviva, Cecile, Laradi, Sandrine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4528043/
https://www.ncbi.nlm.nih.gov/pubmed/26266097
http://dx.doi.org/10.1016/j.mgene.2015.07.003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4528043/
https://www.ncbi.nlm.nih.gov/pubmed/26266097
http://dx.doi.org/10.1016/j.mgene.2015.07.003

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