High functioning male with fragile X syndrome and fragile X-associated tremor/ataxia syndrome-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

High functioning male with fragile X syndrome and fragile X-associated tremor/ataxia syndrome

Published:2015-04-29 Issue:9 Volume:167 Page:2154-2161
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Basuta Kirin¹,Schneider Andrea²³,Gane Louise²,Polussa Jonathan²³,Woodruff Bryan⁴,Pretto Dalyir¹,Hagerman Randi²³,Tassone Flora¹²

Affiliation:

1. Department of Biochemistry and Molecular Medicine; School of Medicine, University of California; Sacramento California

2. MIND Institute; University of California, Davis, Medical Center; Sacramento California

3. Department of Pediatrics; University of California at Davis Medical Center; Sacramento California

4. Department of Neurology; Mayo Clinic; Scottsdale Arizona

Funder

NICHD

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.37125/fullpdf

Reference48 articles.

1. Prevalence and risk of migraine headaches in adult fragile X premutation carriers;Au;Clin Genet,2013

2. Clinical features of boys with fragile X premutations and intermediate alleles;Aziz;Am J Med Genet B,2003

3. Fragile X syndrome: From protein function to therapy;Bagni;Am J Med Genet A,2013

4. Co-occurring conditions associated with FMR1 gene variations: Findings from a national parent survey;Bailey;Am J Med Genet A,2008

5. Distribution of fragile X mental retardation protein in the human auditory brainstem;Beebe;Neuroscience,2014

Cited by 25 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. Unmethylated Mosaic Full Mutation Males without Fragile X Syndrome;Genes;2024-03-03

2. High performing male with fragile X syndrome with an unmethylated FMR1 full mutation: The relevance of clinical and genetic correlations;Clinical Case Reports;2023-06

3. Spectrum of Syndromal Disorders Associated with Expansion of CGG Repeats of the FMR1 Gene Promoter: Pathogenetic Mechanisms and Clinical Manifestations;Neuroscience and Behavioral Physiology;2023-02-21

4. THE SPECTRUM OF SYNDROMIC DISORDERS ASSOCIATED WITH EXPANSION OF CGG-REPEATS IN THE FMR1 PROMOTER: PATHOGENETIC MECHANISMS AND CLINICAL SYMPTOMS;ZH VYSSH NERV DEYAT+;2022

5. The association between mosaicism type and cognitive and behavioral functioning among males with fragile X syndrome;American Journal of Medical Genetics Part A;2021-12-08

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3