Loss-of-Function Mutations in YY1AP1 Lead to Grange Syndrome and a Fibromuscular Dysplasia-Like Vascular Disease-Reference-Cited by-同舟云学术

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Loss-of-Function Mutations in YY1AP1 Lead to Grange Syndrome and a Fibromuscular Dysplasia-Like Vascular Disease

Published:2017-01 Issue:1 Volume:100 Page:21-30
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Guo Dong-chuan,Duan Xue-Yan,Regalado Ellen S.,Mellor-Crummey Lauren,Kwartler Callie S.,Kim Dong,Lieberman Kenneth,de Vries Bert B.A.,Pfundt Rolph,Schinzel Albert,Kotzot Dieter,Shen Xuetong,Yang Min-Lee,Bamshad Michael J.,Nickerson Deborah A.,Gornik Heather L.,Ganesh Santhi K.,Braverman Alan C.,Grange Dorothy K.,Milewicz Dianna M.

Funder

National Heart, Lung and Blood Institute

Vivian L. Smith Foundation

Henrietta B. and Frederick H. Bugher Foundation

National Human Genome Research Institute

National Heart, Lung and Blood Institute Resequencing and Genotyping Service

NIH, National Center for Research Resources

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference31 articles.

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3. Arterial fibrodysplasia. Histopathologic character and current etiologic concepts;Stanley;Arch. Surg.,1975

4. Association between 2 angiographic subtypes of renal artery fibromuscular dysplasia and clinical characteristics;Savard;Circulation,2012

5. Possible familial origin of multifocal renal artery fibromuscular dysplasia;Pannier-Moreau;J. Hypertens.,1997

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