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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Bibliographische Detailangaben
Hauptverfasser: Dastsooz, Hassan, Imanieh, Mohammad Hadi, Dehghani, Seyed Mohsen, Haghighat, Mahmood, Moini, Maryam, Fardaei, Majid
Format: Artigo
Sprache:Inglês
Veröffentlicht: Kowsar 2013
Schlagworte:
Research Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3753551/
https://ncbi.nlm.nih.gov/pubmed/24003324
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5812/hepatmon.8375
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