Associated Papers
Novel familial KDF1 mutation detected in members of a three-generation family with clinical manifestations of ectodermal dysplasia: A report of four cases.
Keramida C et al.
Biomedical Reports, 2025
Tooth agenesis related to a novel KDF1 variant: A case report and literature review.
Intarak N et al.
Oral Diseases, 2024
Gain-of-function variants in the KDF1 gene cause hidradenitis suppurativa associated with ectodermal dysplasia by stabilizing IκB kinase α.
Ziegler A et al.
The British Journal of Dermatology, 2023
KDF1 Novel Variant Causes Unique Dental and Oral Epithelial Defects.
Yu M et al.
International Journal of Molecular Sciences, 2022
Identification of a novel missense heterozygous mutation in the KDF1 gene for non-syndromic congenital anodontia.
Pan Y et al.
Clinical Oral Investigations, 2022
A novel de novo mutation substantiates KDF1 as a gene causing ectodermal dysplasia.
Manaspon C et al.
The British Journal of Dermatology, 2019
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