A Retrospective Study of Clinical and Mutational Findings in 45 Danish Families with Ectodermal Dysplasia
Author:
Publisher
Medical Journals Sweden AB
Subject
Dermatology,General Medicine
Cited by 9 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. A novel homozygous nonsense mutation in NECTIN4 gene in a Pakistani family with ectodermal dysplasia syndactyly syndrome 1;Anais Brasileiros de Dermatologia;2023-09
2. Gene Mutations of the Three Ectodysplasin Pathway Key Players (EDA, EDAR, and EDARADD) Account for More than 60% of Egyptian Ectodermal Dysplasia: A Report of Seven Novel Mutations;Genes;2021-09-08
3. Ectodermal Dysplasia-Syndactyly Syndrome with Toe-Only Minimal Syndactyly Due to a Novel Mutation in NECTIN4: A Case Report and Literature Review;Genes;2021-05-17
4. Turkish Ectodermal Dysplasia Cohort: From Phenotype to Genotype in 17 Families;Cytogenetic and Genome Research;2019
5. A novel homozygous missense variant in NECTIN4 (PVRL4) causing ectodermal dysplasia cutaneous syndactyly syndrome;Annals of Human Genetics;2018-02-12
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