massarray mutation detection (Sequenom)
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Massarray Mutation Detection, supplied by Sequenom, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/massarray+detection+system/massarray+mutation+detection/pm20486126-7-1-0
Average 90 stars, based on 1 article reviews
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Mutagenesis:Article Title: A new approach to long QT syndrome mutation detection by Sequenom MassARRAY system. Article Snippet: Congenital long QT syndrome is an inherited cardiac disorder characterized by a prolonged QT interval and polymorphic ventricular arrhythmias that could result in recurrent syncope, seizures or sudden death as the most dramatic event.. Until now QT interval mutations have been described in 12 genes, where the majority of mutations reside in three genes KCNQ1, KCNH2, and SCN5A.. Diagnosis and prognosis are directly related with the gene and mutation involved. |

