Left ventricular dysfunction in a patient with Angelman syndrome

被引:0
作者
Powell, Adam W. [1 ]
Taylor, Michael D. [1 ]
Hopkin, Robert J. [2 ]
Sublett, Juli [1 ]
Jefferies, John L. [1 ]
机构
[1] Cincinnati Childrens Hosp Med Ctr, Inst Heart, Dept Pediat Cardiol, Cincinnati, OH 45229 USA
[2] Cincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH 45229 USA
关键词
D O I
10.1097/MCD.0000000000000203
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:21 / 22
页数:2
相关论文
共 7 条
[1]   Angelman syndrome: review of clinical and molecular aspects [J].
Bird, Lynne M. .
APPLICATION OF CLINICAL GENETICS, 2014, 7 :93-104
[2]   Angelman syndrome: evolution of the phenotype in adolescents and adults [J].
Clayton-Smith, J .
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2001, 43 (07) :476-480
[3]   Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes [J].
Kalsner, Louisa ;
Chamberlain, Stormy J. .
PEDIATRIC CLINICS OF NORTH AMERICA, 2015, 62 (03) :587-+
[4]   UBE3A/E6-AP mutations cause Angelman syndrome [J].
Kishino, T ;
Lalande, M ;
Wagstaff, J .
NATURE GENETICS, 1997, 15 (01) :70-73
[5]   Angelman Syndrome in Adulthood [J].
Larson, Anna M. ;
Shinnick, Julianna E. ;
Shaaya, Elias A. ;
Thiele, Elizabeth A. ;
Thibert, Ronald L. .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2015, 167 (02) :331-344
[6]  
Sandanam T, 1997, AM J MED GENET, V70, P415, DOI 10.1002/(SICI)1096-8628(19970627)70:4<415::AID-AJMG16>3.0.CO
[7]  
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