Novel LMNA mutation in a patient with progeroid phenotype-Reference-Cited by-同舟云学术

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Novel LMNA mutation in a patient with progeroid phenotype

Published:2015-07-30 Issue:02 Volume:05 Page:143-148
ISSN:1304-2580
Container-title:Journal of Pediatric Neurology
language:en
Short-container-title:J Pediatr Neurol

Author:

Lehwald Lenora¹,Renaud Deborah¹,Campeau Norbert²,Babovic-Vuksanovic Dusica³

Affiliation:

1. Division of Child and Adolescent Neurology, Departments of Neurology and Pediatrics and Adolescent Medicine, Mayo College of Medicine, Rochester, MN, USA

2. Department of Radiology, Mayo College of Medicine, Rochester, MN, USA

3. Department of Medical Genetics, Mayo College of Medicine, Rochester, MN, USA

Publisher

Georg Thieme Verlag KG

Subject

Neurology (clinical),Pediatrics, Perinatology and Child Health

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0035-1557377.pdf

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Atypical Progeria Primarily Manifesting as Premature Cardiac Valvular Disease Segregates with LMNA-Gene Variants;Journal of Cardiovascular Development and Disease;2024-03-05

2. Bilateral stenosis of carotid siphon in Hutchinson-Gilford progeria syndrome;Brain and Development;2013-08

3. An inheritedLMNAgene mutation in atypical Progeria syndrome;American Journal of Medical Genetics Part A;2012-09-18

4. LMNA mutation in progeroid syndrome in association with strokes;European Journal of Medical Genetics;2011-11

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