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Comment
. 2014 Jan 2;94(1):153-4.
doi: 10.1016/j.ajhg.2013.11.016.

Loss of PRDM16 is unlikely to cause cardiomyopathy in 1p36 deletion syndrome

Nicole de Leeuw  1 , Gunnar Houge  2
Affiliations
Comment

Loss of PRDM16 is unlikely to cause cardiomyopathy in 1p36 deletion syndrome

Nicole de Leeuw et al. Am J Hum Genet. .
No abstract available

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Comment in

  • Reponse to De Leeuw and Houge.
    Arndt AK, Macrae CA, Klaassen S. Arndt AK, et al. Am J Hum Genet. 2014 Jan 2;94(1):154-5. doi: 10.1016/j.ajhg.2013.11.011. Am J Hum Genet. 2014. PMID: 24387996 Free PMC article. No abstract available.

Comment on

  • Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.
    Arndt AK, Schafer S, Drenckhahn JD, Sabeh MK, Plovie ER, Caliebe A, Klopocki E, Musso G, Werdich AA, Kalwa H, Heinig M, Padera RF, Wassilew K, Bluhm J, Harnack C, Martitz J, Barton PJ, Greutmann M, Berger F, Hubner N, Siebert R, Kramer HH, Cook SA, MacRae CA, Klaassen S. Arndt AK, et al. Am J Hum Genet. 2013 Jul 11;93(1):67-77. doi: 10.1016/j.ajhg.2013.05.015. Epub 2013 Jun 13. Am J Hum Genet. 2013. PMID: 23768516 Free PMC article.

References

    1. 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. Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy. Am. J. Hum. Genet. 2013;93:67–77. - PMC - PubMed
    1. Keppler-Noreuil K.M., Carroll A.J., Finley W.H., Rutledge S.L. Chromosome 1p terminal deletion: report of new findings and confirmation of two characteristic phenotypes. J. Med. Genet. 1995;32:619–622. - PMC - PubMed

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