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A KRT6A and a Novel KRT16 Gene Mutations in Chinese Patients with Pachyonychia Congenita
BACKGROUND: Pachyonychia congenita (PC) is a rare, autosomal dominant genodermatosis characterized by palmoplantar keratoderma, nail dystrophy, cystic lesions, follicular hyperkeratosis, mucosal leukokeratoses, hyperhidrosis, hoarseness, and, rarely, natal teeth. Five keratin genes, KRT6A, KRT6B, KR...
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| Pubblicato in: | Int J Gen Med |
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| Autori principali: | , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Dove
2021
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7982554/ https://ncbi.nlm.nih.gov/pubmed/33762842 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/IJGM.S280160 |
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