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A de novo variant in the ASPRV1 gene in a dog with ichthyosis
Ichthyoses are a heterogeneous group of inherited cornification disorders characterized by generalized dry skin, scaling and/or hyperkeratosis. Ichthyosis vulgaris is the most common form of ichthyosis in humans and caused by genetic variants in the FLG gene encoding filaggrin. Filaggrin is a key pl...
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| Publicado en: | PLoS Genet |
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| Main Authors: | , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Public Library of Science
2017
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5352138/ https://ncbi.nlm.nih.gov/pubmed/28249031 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1006651 |
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