OR18-01 Massively Parallel Functional Assay Of Extracellular Insulin Receptor Variants

Disclosure: V. Aslanzadeh: None. G. Brierley: None. G. Kudla: None. R.K. Semple: None. Loss-of-function mutations in the gene for the human insulin receptor, INSR, cause either autosomal dominant or autosomal recessive severe insulin resistance. Biallelic mutations produce extreme insulin resistance...

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Detalles Bibliográficos
Autores principales: Aslanzadeh, Vahid, Brierley, Gemma, Kudla, Grzegorz, Kenneth Semple, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Diabetes And Glucose Metabolism
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10555934/
http://dx.doi.org/10.1210/jendso/bvad114.893

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10555934/
http://dx.doi.org/10.1210/jendso/bvad114.893

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