Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.

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Description scientific article published on 13 June 2013
Author/s

author: Sebastian Schäfer  Katharina Wassilew  Matthias Heinig  Paul J Barton  Jörg-Detlef Drenckhahn  Eva Klopocki  Almuth Caliebe  Felix Berger 

Publication date June 13, 2013
Language English
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