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Complex Inheritance of Rare Missense Variants in PAK2, TAP2, and PLCL1 Genes in a Consanguineous Arab Family With Multiple Autoimmune Diseases Including Celiac Disease

BackgroundAutoimmune diseases (AIDs) share a common molecular etiology and often present overlapping clinical presentations. Thus, this study aims to explore the complex molecular basis of AID by whole exome sequencing and computational biology analysis.MethodsMolecular screening of the consanguineo...

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Detaylı Bibliyografya
Asıl Yazarlar: Arwa Mastoor Alharthi, Babajan Banaganapalli, Sabah M. Hassan, Omran Rashidi, Bandar Ali Al-Shehri, Meshari A. Alaifan, Bakr H. Alhussaini, Hadeel A. Alsufyani, Kawthar Saad Alghamdi, Khalda Khalid Nasser, Yagoub Bin-Taleb, Ramu Elango, Noor Ahmad Shaik, Omar I. Saadah
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Frontiers Media S.A. 2022-06-01
Seri Bilgileri:Frontiers in Pediatrics
Konular:
Online Erişim:https://www.frontiersin.org/articles/10.3389/fped.2022.895298/full
Etiketler: Etiketle
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