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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...

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Foilsithe in:Genes (Basel)
Main Authors: Christen, Matthias, Austel, Michaela, Banovic, Frane, Jagannathan, Vidhya, Leeb, Tosso
Formáid: Artigo
Teanga:Inglês
Foilsithe: MDPI 2020
Ábhair:
Rochtain Ar Líne: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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