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- Deciphering the pathogenesis of central centrifugal cicatricial alopecia
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- Genetic Fate Mapping Using Site-Specific Recombinases
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- Case Report: PTCH1 splice-site mutation and sonidegib treatment in Gorlin-Goltz syndrome: clinical insights from a family case study
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
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