Array-Based Resequencing Assay for Mutations Causing Hypertrophic Cardiomyopathy

Background: Dissecting the complex genetic basis of hypertrophic cardiomyopathy (HCM) may be key to both better understanding and optimally managing this most prevalent genetic cardiovascular disease. An array-based resequencing (ABR) assay was developed to facilitate genetic testing in HCM. Methods...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Clin Chem
Päätekijät: Waldmüller, Stephan, Müller, Melanie, Rackebrandt, Kirsten, Binner, Priska, Poths, Sven, Bonin, Michael, Scheffold, Thomas
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Oxford University Press 2008
Aiheet:
Molecular Diagnostics and Genetics
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC7108484/
https://ncbi.nlm.nih.gov/pubmed/18258667
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1373/clinchem.2007.099119
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