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Genetically altered animal models for ATP1A3-related disorders
Within the past 20 years, particularly with the advent of exome sequencing technologies, autosomal dominant and de novo mutations in the gene encoding the neurone-specific α(3) subunit of the Na(+),K(+)-ATPase (NKA α(3)) pump, ATP1A3, have been identified as the cause of a phenotypic continuum of ra...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Company of Biologists Ltd
2021
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8503543/ https://www.ncbi.nlm.nih.gov/pubmed/34612482 http://dx.doi.org/10.1242/dmm.048938 |