Erythrokeratoderma variabilis (EKV) – First Nepalese case documenting GJB3 mutation-Reference-Cited by-同舟云学术

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Erythrokeratoderma variabilis (EKV) – First Nepalese case documenting GJB3 mutation

Published:2021-08-17 Issue:4 Volume:1 Page:
ISSN:2690-442X
Container-title:Skin Health and Disease
language:en
Short-container-title:Skin Health and Disease

Author:

Shah M.¹^ORCID,Baral S.¹²,Adhikari R. C.³

Affiliation:

1. Department of Dermatology Anandaban Hospital The Leprosy Mission Nepal Lalitpur Nepal

2. Department of Pathology Anandaban Hospital The Leprosy Mission Nepal Lalitpur Nepal

3. Department of Pathology Institute of Medicine Maharajgunj Medical Campus Tribhuvan University Kathmandu Nepal

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ski2.63

Reference10 articles.

1. Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis

2. Genetic Heterogeneity in Erythrokeratodermia Variabilis: Novel Mutations in the Connexin Gene GJB4 (Cx30.3) and Genotype-Phenotype Correlations

3. Dominant De Novo Mutations in GJA1 Cause Erythrokeratodermia Variabilis et Progressiva, without Features of Oculodentodigital Dysplasia

4. Clinical and Genetic Heterogeneity of Erythrokeratoderma Variabilis

5. Mutation in the Gene for Connexin 30.3 in a Family with Erythrokeratodermia Variabilis

Cited by 2 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. The GJB3 correlates with the prognosis, immune cell infiltration, and therapeutic responses in lung adenocarcinoma;Open Medicine;2024-01-01

2. Congenital Ichthyosis: Clinical and Genetic Characteristics of the Disease;Current Pediatrics;2022-11-07

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