Case of mild X-linked ichthyosis complicated with paroxysmal supraventricular tachycardia and anemia-Reference-Cited by-同舟云学术

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Case of mild X-linked ichthyosis complicated with paroxysmal supraventricular tachycardia and anemia

Published:2018-03-22 Issue:10 Volume:45 Page:e275-e276
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Maki Yuki¹,Takeichi Takuya¹^ORCID,Kono Michihiro¹^ORCID,Tanaka Yoshihito²,Akiyama Masashi¹^ORCID

Affiliation:

1. Department of Dermatology; Nagoya University Graduate School of Medicine; Nagoya Japan

2. Department of Dermatology; Chukyo Hospital; Nagoya Japan

Funder

Advanced Research and Development Programs for Medical Innovation (AMED-CREST)

Japan Agency for Medical Research and Development

Grant-in-Aid for Scientific Research (B)

Grant-in-Aid for Young Scientists (B)

Japan Society for the Promotion of Science

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/1346-8138.14307/fullpdf

Reference4 articles.

1. Inherited ichthyosis: non-syndromic forms;Takeichi;J Dermatol,2016

2. Novel indel mutation of STS underlies a new phenotype of self-healing recessive X-linked ichthyosis;Takeichi;J Dermatol Sci,2015

3. The phenotype spectrum of X-linked ichthyosis identified by chromosomal microarray;Hand;J Am Acad Dermatol,2015

Cited by 3 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. Characterising heart rhythm abnormalities associated with Xp22.31 deletion;Journal of Medical Genetics;2022-11-15

2. Sex-linked genetic mechanisms and atrial fibrillation risk;European Journal of Medical Genetics;2022-04

3. Medical and neurobehavioural phenotypes in carriers of X-linked ichthyosis-associated genetic deletions in the UK Biobank;Journal of Medical Genetics;2020-03-05

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