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

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

10.1016/j.ajhg.2013.05.015

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Bibliographic Details
Main Authors: Arndt A.-K., Schafer S., Drenckhahn J.-D., Sabeh M.K., Plovie E.R., Caliebe A., Klopocki E., Musso G., Werdich A.A., Kalwa H., Heinig M., Padera R.F., Wassilew K., Bluhm J., Harnack C., Martitz J., Barton P.J., Greutmann M., Berger F., Hubner N., Siebert R., Kramer H.-H., Cook S.A., Macrae C.A., Klaassen S.
Other Authors: DUKE-NUS MEDICAL SCHOOL
Format: Article
Published: 2019
Online Access:http://scholarbank.nus.edu.sg/handle/10635/150858
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Institution: National University of Singapore
Description
Summary:10.1016/j.ajhg.2013.05.015

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