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Cohen syndrome coincident with epidermolytic palmoplantar keratoderma caused by novel KRT9 gene mutation: A rare case report

Cohen syndrome coincident with epidermolytic palmoplantar keratoderma caused by novel KRT9 gene mutation: A rare case report

Bibliographic Details
Main Authors: Yanping Shu, Yongzhe Hou, Qin Zhang
Format: Article
Language:English
Published: Elsevier 2023-12-01
Series:Asian Journal of Surgery
Subjects:
VPS13B gene
Cohen syndrome
KRT9 gene
Epidermolytic palmoplantar keratoderma
Genetic mutation
Online Access:http://www.sciencedirect.com/science/article/pii/S1015958423013829
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http://www.sciencedirect.com/science/article/pii/S1015958423013829

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