Whole-Exome Sequencing for Identification of Genetic Variants Involved in Vitamin D Metabolic Pathways in Families With Vitamin D Deficiency in Saudi Arabia.

Alharazy, Shatha; Naseer, Muhammad Imran; Alissa, Eman; Robertson, Margaret Denise; Lanham-New, Susan; Chaudhary, Adeel G

Alharazy, Shatha; Naseer, Muhammad Imran; Alissa, Eman; Robertson, Margaret Denise; Lanham-New, Susan; Chaudhary, Adeel G.

Afiliación

Alharazy S; Department of Physiology, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Naseer MI; Center of Excellence in Genomic Medicine Research, King Abdulaziz University, Jeddah, Saudi Arabia.
Alissa E; Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
Robertson MD; Department of Clinical Biochemistry, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia.
Lanham-New S; Department of Nutritional Sciences, Faculty of Health and Medical Sciences, University of Surrey, Guildford, United Kingdom.
Chaudhary AG; Department of Nutritional Sciences, Faculty of Health and Medical Sciences, University of Surrey, Guildford, United Kingdom.

Front Genet ; 12: 677780, 2021.

Article en En | MEDLINE | ID: mdl-34168679

Palabras clave

Saudi Arabia; family study; polymorphisms; variants; vitamin D; vitamin D deficiency; vitamin D metabolism; whole-exome sequencing

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Front Genet Año: 2021 Tipo del documento: Article País de afiliación: Arabia Saudita Pais de publicación: Suiza

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