A novel custom resequencing array for dilated cardiomyopathy

Genetic tests for the most commonly mutated genes in dilated cardiomyopathy (DCM) can confirm a clinical diagnosis in the proband and inform family management. Presymptomatic family members can be identified, allowing for targeted clinical monitoring to minimize adverse outcomes. However, the marked...

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Veröffentlicht in:	Genetics in medicine 2010-05, Vol.12 (5), p.268-278
Hauptverfasser:	Zimmerman, Rebekah S., Cox, Stephanie, Lakdawala, Neal K., Cirino, Allison, Mancini-Dinardo, Debora, Clark, Eugene, Leon, Annette, Duffy, Elizabeth, White, Emily, Baxter, Samantha, Alaamery, Manal, Farwell, Lisa, Weiss, Scott, Seidman, Christine E., Seidman, Jonathan G., Ho, Carolyn Y., Rehm, Heidi L., Funke, Birgit H.
Format:	Artikel
Sprache:	eng
Schlagworte:	Biomedical and Life Sciences Biomedicine Cardiomyopathy, Dilated - diagnosis Cardiomyopathy, Dilated - genetics dilated cardiomyopathy Family Female genetic test Genetic Testing Human Genetics Humans Laboratory Medicine locus heterogeneity Mutation Pregnancy resequencing array
Online-Zugang:	Volltext
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