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Noncompaction of the Ventricular Myocardium Is Associated with a De Novo Mutation in the β-Myosin Heavy Chain Gene

Posted on 2013-02-21 - 11:16

Family members are shown by filled black symbols (affected), by half filled symbols (partially affected), open symbols (unaffected) and gray symbols (unknown affection status). An arrow points to the index patient. The disease associated haplotype is shown by filled black bars. Markers within the minimum disease associated haplotype are boxed. Below the haplotypes of each individual the occurrence of wild-type (+) and mutant MYH7 alleles (−) is indicated.

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AUTHORS (18)

Birgit S. Budde
Priska Binner
Stephan Waldmüller
Wolfgang Höhne
Wulf Blankenfeldt
Sabine Hassfeld
Jürgen Brömsen
Anastassia Dermintzoglou
Marcus Wieczorek
Erik May
Elisabeth Kirst
Carmen Selignow
Kirsten Rackebrandt
Melanie Müller
Roger S. Goody
Hans-Peter Vosberg
Peter Nürnberg
Thomas Scheffold
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