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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...
Tallennettuna:
| Julkaisussa: | Genes (Basel) |
|---|---|
| Päätekijät: | , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
MDPI
2020
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7716214/ https://ncbi.nlm.nih.gov/pubmed/33143176 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/genes11111297 |
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