Whole Exome Sequencing Identifies a Rare Mutation in NACAD as a Possible Cause of COVID Orchitis in Brothers.

Reddy, Rohit; Efimenko, Iakov; Chertman, Willy; Kohn, Taylor; Diaz, Parris; Seetharam, Deepa; Khodamoradi, Kajal; Kresch, Eliyahu; Ramasamy, Ranjith

Reddy, Rohit; Efimenko, Iakov; Chertman, Willy; Kohn, Taylor; Diaz, Parris; Seetharam, Deepa; Khodamoradi, Kajal; Kresch, Eliyahu; Ramasamy, Ranjith.

Afiliación

Reddy R; Miller School of Medicine, University of Miami 1120 NW 14th Street, Miami, FL.
Efimenko I; Miller School of Medicine, University of Miami 1120 NW 14th Street, Miami, FL.
Chertman W; Miller School of Medicine, University of Miami 1120 NW 14th Street, Miami, FL.
Kohn T; The James Buchanan Brady Urological Institute and Department of Urology, Johns Hopkins University School of Medicine, Baltimore, MD.
Diaz P; Department of Urology, University of Miami Miller School of Medicine, Miami, FL.
Seetharam D; Department of Urology, University of Miami Miller School of Medicine, Miami, FL.
Khodamoradi K; Department of Urology, University of Miami Miller School of Medicine, Miami, FL.
Kresch E; Department of Urology, University of Miami Miller School of Medicine, Miami, FL.
Ramasamy R; Department of Urology, University of Miami Miller School of Medicine, Miami, FL. Electronic address: Ramasamy@miami.edu.

Urology ; 159: 83-86, 2022 01.

Article en En | MEDLINE | ID: mdl-34678309

Asunto(s)

COVID-19/complicaciones; Deleción Cromosómica; Cromosomas Humanos Par 7; Secuenciación del Exoma; Orquitis/virología; Adulto; Enzima Convertidora de Angiotensina 2/sangre; Mutación del Sistema de Lectura; Humanos; Masculino; Hermanos

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Orquitis / Cromosomas Humanos Par 7 / Deleción Cromosómica / Secuenciación del Exoma / COVID-19 Tipo de estudio: Prognostic_studies Límite: Adult / Humans / Male Idioma: En Revista: Urology Año: 2022 Tipo del documento: Article

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