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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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

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spelling	sg-nus-scholar.10635-1508582024-11-13T09:12:31Z Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy 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. DUKE-NUS MEDICAL SCHOOL 10.1016/j.ajhg.2013.05.015 American Journal of Human Genetics 93 1 67-77 AJHGA 2019-01-15T08:26:31Z 2019-01-15T08:26:31Z 2013 Article 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. (2013). Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy. American Journal of Human Genetics 93 (1) : 67-77. ScholarBank@NUS Repository. https://doi.org/10.1016/j.ajhg.2013.05.015 29297 http://scholarbank.nus.edu.sg/handle/10635/150858 Scopus
institution	National University of Singapore
building	NUS Library
continent	Asia
country	Singapore Singapore
content_provider	NUS Library
collection	ScholarBank@NUS
description	10.1016/j.ajhg.2013.05.015
author2	DUKE-NUS MEDICAL SCHOOL
author_facet	DUKE-NUS MEDICAL SCHOOL 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.
format	Article
author	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.
spellingShingle	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. Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy
author_sort	Arndt A.-K.
title	Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy
title_short	Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy
title_full	Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy
title_fullStr	Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy
title_full_unstemmed	Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy
title_sort	fine mapping of the 1p36 deletion syndrome identifies mutation of prdm16 as a cause of cardiomyopathy
publishDate	2019
url	http://scholarbank.nus.edu.sg/handle/10635/150858
_version_	1821189958090620928

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

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