The first Japanese family of CDH3 ‐related hypotrichosis with juvenile macular dystrophy-Reference-Cited by-同舟云学术

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The first Japanese family of CDH3 ‐related hypotrichosis with juvenile macular dystrophy

Published:2021-04-09 Issue:6 Volume:9 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Hayashi Takaaki¹²^ORCID,Katagiri Satoshi¹,Kubota Daiki³,Mizobuchi Kei¹^ORCID,Ishiuji Yozo⁴,Asahina Akihiko⁴^ORCID,Kameya Shuhei³,Nakano Tadashi¹

Affiliation:

1. Department of Ophthalmology The Jikei University School of Medicine Tokyo Japan

2. Department of Ophthalmology Katsushika Medical CenterThe Jikei University School of Medicine Tokyo Japan

3. Department of Ophthalmology Nippon Medical School Chiba Hokusoh Hospital Chiba Japan

4. Department of Dermatology The Jikei University School of Medicine Tokyo Japan

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1688

Reference23 articles.

1. The cadherin superfamily: diversity in form and function

2. CDH3-Related Syndromes: Report on a New Mutation and Overview of the Genotype-Phenotype Correlations

3. Characterization ofCDH3-Related Congenital Hypotrichosis With Juvenile Macular Dystrophy

4. A Missense Mutation in CDH3, Encoding P-Cadherin, Causes Hypotrichosis with Juvenile Macular Dystrophy

5. Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy

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. Multimodal imaging analysis of autosomal recessive bestrophinopathy: Case series;Medicine;2024-07-19

2. <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case;Current Pediatrics;2023-11-05

3. Bardet–Biedl syndrome associated with novel compound heterozygous variants in BBS12 gene;Documenta Ophthalmologica;2022-12-27

4. The first reported case of CDH3-related hypotrichosis with juvenile macular dystrophy from Jordan: a case report;Ophthalmic Genetics;2022-01-17

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