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Heterozygous frameshift mutation in keratin 5 in a family with Galli–Galli disease
BACKGROUND: Reticulate pigmentary disorders include the rare autosomal dominant Galli–Galli disease (GGD) and Dowling–Degos disease (DDD). Clinical diagnosis between some of the subtypes can be difficult due to a degree of overlap between clinical features, therefore analysis at the molecular level...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Publishing Ltd
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4150463/ https://ncbi.nlm.nih.gov/pubmed/24372084 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bjd.12813 |
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