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 α3 subunit of the Na+,K+-ATPase (NKA α3) pump, ATP1A3, have been identified as the cause of a phenotypic continuum of rare neuro...

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Main Authors: Hannah W. Y. Ng (Author), Jennifer A. Ogbeta (Author), Steven J. Clapcote (Author)
Format: Book
Published: The Company of Biologists, 2021-10-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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