Assessing Human Genetic Variations in Glucose Transporter SLC2A10 and Their Role in Altering Structural and Functional Properties

Purpose: Demand is increasing for clinical genomic sequencing to provide diagnoses for patients presenting phenotypes indicative of genetic diseases, but for whom routine genetic testing failed to yield a diagnosis. DNA-based testing using high-throughput technologies often identifies variants with...

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Detalles Bibliográficos
Autores principales: Zimmermann, Michael T., Urrutia, Raul, Cousin, Margot A., Oliver, Gavin R., Klee, Eric W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068234/
https://www.ncbi.nlm.nih.gov/pubmed/30090112
http://dx.doi.org/10.3389/fgene.2018.00276

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6068234/
https://www.ncbi.nlm.nih.gov/pubmed/30090112
http://dx.doi.org/10.3389/fgene.2018.00276

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