NSDHL Frameshift Deletion in a Mixed Breed Dog with Progressive Epidermal Nevi

Loss-of-function variants in the NSDHL gene have been associated with epidermal nevi in humans with congenital hemidysplasia, ichthyosiform nevi, and limb defects (CHILD) syndrome and in companion animals. The NSDHL gene codes for the NAD(P)-dependent steroid dehydrogenase-like protein, which is inv...

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Detalles Bibliográficos
Autores principales: Christen, Matthias, Austel, Michaela, Banovic, Frane, Jagannathan, Vidhya, Leeb, Tosso
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7716214/
https://www.ncbi.nlm.nih.gov/pubmed/33143176
http://dx.doi.org/10.3390/genes11111297

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7716214/
https://www.ncbi.nlm.nih.gov/pubmed/33143176
http://dx.doi.org/10.3390/genes11111297

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