Exon Sequencing of PKD1 Gene in an Iranian Patient with Autosomal-Dominant Polycystic Kidney Disease

Introduction: Autosomal dominant polycystic kidney disease (ADPKD) is one of the most common genetic kidney disorders with the incidence of 1 in 1,000 births. ADPKD is genetically heterogeneous with two genes identified: PKD1 (16p13.3, 46 exons) and PKD2 (4q21, 15 exons). Eighty five percent of the...

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Detalles Bibliográficos
Autores principales: Hafizi, Atousa, Khatami, Saeid Reza, Galehdari, Hamid, Shariati, Gholamreza, Saberi, Ali Hossein, Hamid, Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Pasteur Institute of Iran 2014
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4048478/
https://www.ncbi.nlm.nih.gov/pubmed/24842140
http://dx.doi.org/10.6091/ibj.1317.2014

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4048478/
https://www.ncbi.nlm.nih.gov/pubmed/24842140
http://dx.doi.org/10.6091/ibj.1317.2014

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