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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:PLoS Genet
Prif Awduron: Bauer, Anina, Waluk, Dominik P., Galichet, Arnaud, Timm, Katrin, Jagannathan, Vidhya, Sayar, Beyza S., Wiener, Dominique J., Dietschi, Elisabeth, Müller, Eliane J., Roosje, Petra, Welle, Monika M., Leeb, Tosso
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Public Library of Science 2017
Pynciau:
Research Article
Mynediad Ar-lein: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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