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引用本文的文献

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本文引用的文献

1
Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy.1p36 缺失综合征的精细定位确定 PRDM16 突变是心肌病的一个原因。
Am J Hum Genet. 2013 Jul 11;93(1):67-77. doi: 10.1016/j.ajhg.2013.05.015. Epub 2013 Jun 13.
2
Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation.60例1p36缺失综合征患者的进一步描述：一种可识别的表型及发育迟缓与智力障碍的常见病因
Pediatrics. 2008 Feb;121(2):404-10. doi: 10.1542/peds.2007-0929.
3
Noncompaction of the left ventricle: primary cardiomyopathy with an elusive genetic etiology.左心室心肌致密化不全：一种病因不明的原发性心肌病。
Curr Opin Pediatr. 2007 Dec;19(6):619-27. doi: 10.1097/MOP.0b013e3282f1ecbc.
4
Monosomy 1p36 deletion syndrome.1p36缺失综合征
Am J Med Genet C Semin Med Genet. 2007 Nov 15;145C(4):346-56. doi: 10.1002/ajmg.c.30154.
5
Left ventricular non-compaction: insights from cardiovascular magnetic resonance imaging.左心室心肌致密化不全：心血管磁共振成像的见解
J Am Coll Cardiol. 2005 Jul 5;46(1):101-5. doi: 10.1016/j.jacc.2005.03.045.
6
Echocardiographic and pathoanatomical characteristics of isolated left ventricular non-compaction: a step towards classification as a distinct cardiomyopathy.孤立性左心室心肌致密化不全的超声心动图及病理解剖特征：迈向将其归类为一种独特心肌病的一步。
Heart. 2001 Dec;86(6):666-71. doi: 10.1136/heart.86.6.666.

Left ventricular noncompaction cardiomyopathy: adult association with 1p36 deletion syndrome.

作者信息

Lee James, Rinehart Sarah, Polsani Venkateshewar

机构信息

Piedmont Heart Institute, Atlanta, Georgia.

出版信息

Methodist Debakey Cardiovasc J. 2014 Oct-Dec;10(4):258-9. doi: 10.14797/mdcj-10-4-258.

DOI:10.14797/mdcj-10-4-258
PMID:25624984
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4300068/
Abstract
摘要