Compound Heterozygous Null Variants in <i>ITGB4</i> Gene Causing Severe Phenotype of Junctional Epidermolysis Bullosa With Pyloric Atresia in Thai Newborn: Genotype-Phenotype Correlation From a Case Report and Review of the Literature.

Int J Genomics · 2025 · PMC12482511 · PMID 41035785

Europe PMC DOI

hedged sentence

0.1210

closest p · 2.4× alpha

0.1210

boldest claim

The sentences

borderline significantp = 0.121not close (p > 0.1)

Meanwhile, compound heterozygous PTC or splice site variants in both alleles were associated with a borderline significant increased risk of the lethal form (odds ratio 3.15; 95% CI 0.74–13.45; p = 0.121). 5.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.

Compound Heterozygous Null Variants in &lt;i&gt;ITGB4&lt;/i&gt; Gene Causing Severe Phenotype of Junctional Epidermolysis Bullosa With Pyloric Atresia in Thai Newborn: Genotype-Phenotype Correlation From a Case Report and Review of the Literature.

The sentences

Compound Heterozygous Null Variants in <i>ITGB4</i> Gene Causing Severe Phenotype of Junctional Epidermolysis Bullosa With Pyloric Atresia in Thai Newborn: Genotype-Phenotype Correlation From a Case Report and Review of the Literature.