Association of mannose-binding lectin 2 gene polymorphisms with Guillain-Barré syndrome

Complement activation plays a critical role in the pathogenesis of Guillain-Barré syndrome (GBS), a debilitating immune-mediated neuropathy. Mannose-binding lectin (MBL) is a complement activation factor of lectin pathway which as genetic host factor may influence the susceptibility or severity of G...

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Vydáno v:	Scientific reports Ročník 12; číslo 1; s. 5791 - 11
Hlavní autoři:	Jahan, Israt, Hayat, Shoma, Khalid, Mir M., Ahammad, Rijwan U., Asad, Asaduzzaman, Islam, Badrul, Mohammad, Quazi D., Jacobs, Bart C., Islam, Zhahirul
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	London Nature Publishing Group UK 06.04.2022 Nature Publishing Group Nature Portfolio
Témata:	631/337 692/420 692/53 692/617 Adolescent Adult Complement Activation Exons Gene polymorphism Genetic Predisposition to Disease Genotype Guillain-Barre syndrome Guillain-Barre Syndrome - genetics Haplotypes Heterozygosity Humanities and Social Sciences Humans Lectins Male Mannose Mannose-binding lectin Mannose-Binding Lectin - genetics multidisciplinary Neuropathy Patients Polymorphism, Genetic Science Science (multidisciplinary) Young Adult
ISSN:	2045-2322, 2045-2322
On-line přístup:	Získat plný text
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