Pachyonychia Congenita: A Spectrum of KRT6a Mutations in Australian Patients. [electronic resource]
Producer: 20170331Description: 337-42 p. digitalISSN:- 1525-1470
- Australia
- Child, Preschool
- Dermatologic Agents -- therapeutic use
- Disease Progression
- Drug Therapy, Combination
- Female
- Follow-Up Studies
- Genetic Predisposition to Disease
- Humans
- Keratin-6 -- genetics
- Keratolytic Agents -- therapeutic use
- Leukoplakia, Oral -- drug therapy
- Mutation -- genetics
- Pachyonychia Congenita -- drug therapy
- Rare Diseases
- Risk Assessment
- Treatment Outcome
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Publication Type: Case Reports; Journal Article; Review
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