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Second-hit somatic mutations in mevalonate pathway genes underlie porokeratosis
Familial and sporadic porokeratosis are associated with germline heterozygous mutations in mevalonate pathway genes. Kubo et al. show that each skin lesion of DSAP originates from a postnatal keratinocyte clone with a different second-hit genetic event in the wild type allele of the corresponding ge...
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| Publicado no: | J Invest Dermatol |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2019
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7962864/ https://ncbi.nlm.nih.gov/pubmed/31753123 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jid.2019.07.723 |
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