Onset in the seventh decade and lack of symptoms in heterozygotes for the TTRMet30 mutation in hereditary amyloid neuropathy—type I (Portuguese, Andrade)-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Onset in the seventh decade and lack of symptoms in heterozygotes for the TTRMet30 mutation in hereditary amyloid neuropathy—type I (Portuguese, Andrade)

Published:1987-06 Issue:2 Volume:27 Page:345-357
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Sequeiros Jorge,Saraiva Maria João Mascarenhas,Opitz John M.,Reynolds James F.

Publisher

Wiley

Subject

Genetics(clinical)

Reference48 articles.

1. A PECULIAR FORM OF PERIPHERAL NEUROPATHY

2. (1975): Hereditary amyloid neuropathy. In (eds): “Handbook of Clinical Neurology,” Vol 21. Amsterdam: North Holland Publishing Co., pp 119-143.

3. Hereditary amyloidosis

Cited by 39 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. Anticipation on age at onset in kindreds with hereditary ATTRV30M amyloidosis from the Majorcan cluster;Amyloid;2020-07-07

2. Large normal alleles of ATXN2 decrease age at onset in transthyretin familial amyloid polyneuropathy Val30Met patients;Annals of Neurology;2019-01-29

3. Clinicopathological correlations of sural nerve biopsies in TTR Val30Met familial amyloid polyneuropathy;Brain Communications;2019-01-01

4. Age-dependent cognitive dysfunction in untreated hereditary transthyretin amyloidosis;Journal of Neurology;2017-12-05

5. A Trans-acting Factor May Modify Age at Onset in Familial Amyloid Polyneuropathy ATTRV30M in Portugal;Molecular Neurobiology;2017-05-19

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