Multiplex ARMS PCR to Detect 8 Common Mutations of ATP7B Gene in Patients With Wilson Disease

BACKGROUND: Wilson disease is a rare disorder of copper metabolism due to mutation in ATP7B gene. Proper counseling of patients with Wilson disease, and their families necessitates finding mutation in ATP7B gene. Finding mutations in ATP7B gene with 21 exons, and more than 500 mutations is expensive...

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Detalles Bibliográficos
Autores principales: Dastsooz, Hassan, Imanieh, Mohammad Hadi, Dehghani, Seyed Mohsen, Haghighat, Mahmood, Moini, Maryam, Fardaei, Majid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3753551/
https://www.ncbi.nlm.nih.gov/pubmed/24003324
http://dx.doi.org/10.5812/hepatmon.8375

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3753551/
https://www.ncbi.nlm.nih.gov/pubmed/24003324
http://dx.doi.org/10.5812/hepatmon.8375

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