Whole exome sequencing: Uncovering causal genetic variants for ocular diseases.

Gupta, Shashank; Chatterjee, Souradip; Mukherjee, Ashim; Mutsuddi, Mousumi

Gupta, Shashank; Chatterjee, Souradip; Mukherjee, Ashim; Mutsuddi, Mousumi.

Afiliación

Gupta S; Department of Molecular and Human Genetics, Institute of Science, Banaras Hindu University, Varanasi 221005, India.
Chatterjee S; Department of Molecular and Human Genetics, Institute of Science, Banaras Hindu University, Varanasi 221005, India.
Mukherjee A; Department of Molecular and Human Genetics, Institute of Science, Banaras Hindu University, Varanasi 221005, India.
Mutsuddi M; Department of Molecular and Human Genetics, Institute of Science, Banaras Hindu University, Varanasi 221005, India. Electronic address: mousumi_mutsuddi@yahoo.com.

Exp Eye Res ; 164: 139-150, 2017 11.

Article en En | MEDLINE | ID: mdl-28844620

Asunto(s)

Exoma; Oftalmopatías/genética; Análisis de Secuencia de ADN/métodos; Análisis Mutacional de ADN/métodos; Oftalmopatías/diagnóstico; Proteínas del Ojo/genética; Variación Genética; Humanos

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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Análisis de Secuencia de ADN / Oftalmopatías / Exoma Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Revista: Exp Eye Res Año: 2017 Tipo del documento: Article País de afiliación: India

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