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Antibody Recognition to the Hyperglucosylated Adhesin Protein HMW1ct of Non Typeable <i>Haemophilus Influenzae</i> in Rett Syndrome

2024-07-10

Abstract excerpt

Rett syndrome (RTT) is an X-linked neurodevelopment disorder associated with the single monogenic mutation in methyl-CpG binding protein 2 (MeCP2) in up to 95% of cases. The growing number of genome-wide association studies and incomplete concordance for autoimmune diseases in monozygotic twins concur to support the involvement of environmental factors, like infectious agents or chemicals, in the breakdown of tole...

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Literature Corpus work
83d87e72-94f0-5cf7-894b-9f17e3e475e0
DOI
10.20944/preprints202407.0766.v1
Open publication

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Antibody Recognition to the Hyperglucosylated Adhesin Protein HMW1ct of Non Typeable <i>Haemophilus Influenzae</i> in Rett SyndromeDOI 10.20944/preprints202407.0766.v1
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