Associated Papers
Functional Characterization of a Novel In-Frame Indel and a Founder Variant in SERPINB7 Associated With Palmoplantar Keratoderma.
Liu J et al.
The Journal of Dermatology, 2026
Investigation of Nagashima-type palmoplantar keratoderma in China: A cross-sectional study of 234 patients.
Liu J et al.
The Journal of Dermatology, 2023
Two novel mutations of SERPINB7 in eight cases of Nagashima-type palmoplantar keratosis in the Chinese population.
Xiao T et al.
The Journal of Dermatology, 2022
Nagashima-Type Palmoplantar Keratosis: Clinical Characteristics, Genetic Characterization, and Clinical Management.
Huang C et al.
Biomed Research International, 2021
Identification of a Rare Case With Nagashima-Type Palmoplantar Keratoderma and 18q Deletion Syndrome via Exome Sequencing and Low-Coverage Whole-Genome Sequencing.
Li Q et al.
Frontiers in Genetics, 2021
34616427 (PubMed )
Supplement: Data_Sheet_1.zip › All_the_Supplementary_Materials-2021-09-08 › Supplementary_Tables_and_Figures.docx
Nagashima-type palmoplantar keratoderma and malignant melanoma in Japanese patients.
Korekawa A et al.
The British Journal of Dermatology, 2019
A sporadic case of Nagashima-type palmoplantar keratosis caused by gene mutation in SERPINB7.
Li CX et al.
Clinical and Experimental Dermatology, 2016
Nagashima-Type Palmoplantar Keratosis with Compound Heterozygous Mutations in SERPINB7.
Songsantiphap C et al.
Case Reports in Dermatology, 0
Mutation analysis in three Chinese pedigrees with palmoplantar keratoderma caused by SERPINB7 gene mutations.
Han H et al.
Indian Journal of Dermatology, Venereology and Leprology, 0
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