Prion protein gene mutation detection using long-read Nanopore sequencing.

Kroll, François; Dimitriadis, Athanasios; Campbell, Tracy; Darwent, Lee; Collinge, John; Mead, Simon; Vire, Emmanuelle

Kroll, François; Dimitriadis, Athanasios; Campbell, Tracy; Darwent, Lee; Collinge, John; Mead, Simon; Vire, Emmanuelle.

Afiliación

Kroll F; MRC Prion Unit at University College London (UCL), UCL Institute of Prion Diseases, UCL, London, W1W 7FF, UK.
Dimitriadis A; MRC Prion Unit at University College London (UCL), UCL Institute of Prion Diseases, UCL, London, W1W 7FF, UK.
Campbell T; MRC Prion Unit at University College London (UCL), UCL Institute of Prion Diseases, UCL, London, W1W 7FF, UK.
Darwent L; MRC Prion Unit at University College London (UCL), UCL Institute of Prion Diseases, UCL, London, W1W 7FF, UK.
Collinge J; MRC Prion Unit at University College London (UCL), UCL Institute of Prion Diseases, UCL, London, W1W 7FF, UK.
Mead S; MRC Prion Unit at University College London (UCL), UCL Institute of Prion Diseases, UCL, London, W1W 7FF, UK. s.mead@prion.ucl.ac.uk.
Vire E; MRC Prion Unit at University College London (UCL), UCL Institute of Prion Diseases, UCL, London, W1W 7FF, UK.

Sci Rep ; 12(1): 8284, 2022 05 18.

Article en En | MEDLINE | ID: mdl-35585119

Asunto(s)

Secuenciación de Nanoporos; Enfermedades por Prión; Priones; Animales; Mutación; Enfermedades por Prión/diagnóstico; Enfermedades por Prión/genética; Proteínas Priónicas/genética; Proteínas Priónicas/metabolismo; Priones/genética

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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Priones / Enfermedades por Prión / Secuenciación de Nanoporos Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Animals Idioma: En Revista: Sci Rep Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido

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