Whole-exome sequencing deciphers the genetic profile of visual impairments in patients from Southwest Iran.

Zamani, Mina; Sedighzadeh, Sahar; Seifi, Tahereh; Negahdari, Samira; Zeighami, Jawaher; Sedaghat, Alireza; Shariati, Gholamreza; Galehdari, Hamid

Zamani, Mina; Sedighzadeh, Sahar; Seifi, Tahereh; Negahdari, Samira; Zeighami, Jawaher; Sedaghat, Alireza; Shariati, Gholamreza; Galehdari, Hamid.

Afiliación

Zamani M; Department of Biology, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
Sedighzadeh S; Narges Medical Genetics and Prenatal Diagnosis Laboratory, Ahvaz, Iran.
Seifi T; Department of Biology, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
Negahdari S; Narges Medical Genetics and Prenatal Diagnosis Laboratory, Ahvaz, Iran.
Zeighami J; Department of Biology, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
Sedaghat A; Narges Medical Genetics and Prenatal Diagnosis Laboratory, Ahvaz, Iran.
Shariati G; Narges Medical Genetics and Prenatal Diagnosis Laboratory, Ahvaz, Iran.
Galehdari H; Legal Medicine Research Center, Legal Medicine Organization, Ahvaz, Iran.

Mol Genet Genomics ; 297(5): 1289-1300, 2022 Sep.

Article en En | MEDLINE | ID: mdl-35754085

Asunto(s)

Exoma; Perfil Genético; Estudio de Asociación del Genoma Completo; Humanos; Irán; Mutación; Linaje; Trastornos de la Visión; Secuenciación del Exoma

Palabras clave

Eye disease; NGS; Pathogenic variants; WES

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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Exoma / Perfil Genético Límite: Humans País/Región como asunto: Asia Idioma: En Revista: Mol Genet Genomics Asunto de la revista: BIOLOGIA MOLECULAR / GENETICA Año: 2022 Tipo del documento: Article País de afiliación: Irán

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