A Missense Mutation in CDH3, Encoding P-Cadherin, Causes Hypotrichosis with Juvenile Macular Dystrophy-Reference-Cited by-同舟云学术

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

Published:2002-11 Issue:5 Volume:119 Page:1210-1213
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Indelman Margarita,Bergman Reuven,Petronius Danny,Ciubutaro Dan,Sprecher Eli,Lurie Raziel,Richard Gabriele,Miller Benjamin,Leibu Rina

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference23 articles.

1. Alopecia universalis associated with a mutation in the human hairless gene;Ahmad;Science,1998

2. Expression of E-cadherin by human retinal pigment epithelium: delayed expression in vitro;Burke;Invest Dermatol Vis Sci,1999

3. Cloning, genomic organization, alternative transcripts and mutational analysis of the gene responsible for autosomal recessive universal congenital alopecia;Cichon;Hum Mol Genet,1998

4. An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis;Da Cruz;Br J Opthalmol,2001

5. De novo hair follicle morphogenesis and hair tumors in mice expressing a truncated beta-catenin in skin;Gat;Cell,1998

Cited by 58 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. Clinical, genetic, and electron microscopy of hair findings in a patient with CDH3-related hypotrichosis with juvenile macular dystrophy;Clinical Dysmorphology;2023-02-02

2. Retinal cadherins and the retinal cadherinopathies: Current concepts and future directions;Progress in Retinal and Eye Research;2022-09

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

4. The first Japanese family of CDH3 ‐related hypotrichosis with juvenile macular dystrophy;Molecular Genetics & Genomic Medicine;2021-04-09

5. Hypotrichosis with Juvenile Macular Dystrophy in Saudi Arabia: A Case Report;Skin Appendage Disorders;2020-12-15

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