Matches in Nanopublications for { ?s ?p "[Leukocyte adhesion deficiency type 1 (LAD I) is an autosomal recessive disorder caused by mutations in the ITGB2 gene, encoding the beta2 integrin family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP627084.RAAqYZtJ3DA66w36cxLCuQhhHfLrhmGKBXQ49CFYA3XTg130_assertion description "[Leukocyte adhesion deficiency type 1 (LAD I) is an autosomal recessive disorder caused by mutations in the ITGB2 gene, encoding the beta2 integrin family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP627084.RAAqYZtJ3DA66w36cxLCuQhhHfLrhmGKBXQ49CFYA3XTg130_provenance.
- NP334081.RAnrZe5QyHcaSyRx8h4hPC1-_vo9J-C-MFrPJdAl9pChc130_assertion description "[Leukocyte adhesion deficiency type 1 (LAD I) is an autosomal recessive disorder caused by mutations in the ITGB2 gene, encoding the beta2 integrin family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP334081.RAnrZe5QyHcaSyRx8h4hPC1-_vo9J-C-MFrPJdAl9pChc130_provenance.
- NP3336.RANRXBLb3V5PfZ8eJ32CA3qvVRRXJTA8Pi9yCDPVC9veg130_assertion description "[Leukocyte adhesion deficiency type 1 (LAD I) is an autosomal recessive disorder caused by mutations in the ITGB2 gene, encoding the beta2 integrin family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP3336.RANRXBLb3V5PfZ8eJ32CA3qvVRRXJTA8Pi9yCDPVC9veg130_provenance.
- NP714495.RAgcMsvPKbxjKlJwv3abLFQQVeDohoo_FockW7-eqq5Xk130_assertion description "[Leukocyte adhesion deficiency type 1 (LAD I) is an autosomal recessive disorder caused by mutations in the ITGB2 gene, encoding the beta2 integrin family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP714495.RAgcMsvPKbxjKlJwv3abLFQQVeDohoo_FockW7-eqq5Xk130_provenance.
- NP445598.RAYOCK1pABjmZiRg8cuJts8cV9K4C7z8sGzOAkR6IHObQ130_assertion description "[Leukocyte adhesion deficiency type 1 (LAD I) is an autosomal recessive disorder caused by mutations in the ITGB2 gene, encoding the beta2 integrin family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP445598.RAYOCK1pABjmZiRg8cuJts8cV9K4C7z8sGzOAkR6IHObQ130_provenance.
- assertion description "[Leukocyte adhesion deficiency type 1 (LAD I) is an autosomal recessive disorder caused by mutations in the ITGB2 gene, encoding the beta2 integrin family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.