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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Detalhes bibliográficos
Publicado no:Saudi J Biol Sci
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Elsevier 2020
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7254030/
https://ncbi.nlm.nih.gov/pubmed/32489286
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.sjbs.2020.04.011
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