Whole exome sequencing of a Saudi family and systems biology analysis identifies CPED1 as a putative causative gene to Celiac Disease

Celiac disease (CD) is a gastrointestinal disorder whose genetic basis is not fully understood. Therefore, we studied a Saudi family with two CD affected siblings to discover the causal genetic defect. Through whole exome sequencing (WES), we identified that both siblings have inherited an extremely...

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Detalles Bibliográficos
Autores principales: Bokhari, Hifaa A., Shaik, Noor Ahmad, Banaganapalli, Babajan, Nasser, Khalidah Khalid, Ageel, Hossain Ibrahim, Al Shamrani, Ali Saad, Rashidi, Omran M., Al Ghubayshi, Omar Yaseen, Shaik, Jilani, Ahmad, Aftab, Alrayes, Nuha Mohammad, Al-Aama, Jumana Yousuf, Elango, Ramu, Saadah, Omar Ibrahim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7254030/
https://www.ncbi.nlm.nih.gov/pubmed/32489286
http://dx.doi.org/10.1016/j.sjbs.2020.04.011

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7254030/
https://www.ncbi.nlm.nih.gov/pubmed/32489286
http://dx.doi.org/10.1016/j.sjbs.2020.04.011

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