Matches in Nanopublications for { ?s ?p "[The aim of the study was to search for mutations of SCNN1B and SCNN1G in an Italian family with apparently dominant autosomal transmission of a clinical phenotype consistent with Liddle's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP917866.RAekOwV8pGF7jxA3xtNfVFO7Or8zZR59uoLaZQ-s3zzZM130_assertion description "[The aim of the study was to search for mutations of SCNN1B and SCNN1G in an Italian family with apparently dominant autosomal transmission of a clinical phenotype consistent with Liddle's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917866.RAekOwV8pGF7jxA3xtNfVFO7Or8zZR59uoLaZQ-s3zzZM130_provenance.
- NP661136.RASGYGr6gajTbgMLLWOedmFfVm1My7E9sm60sdlwoGEfA130_assertion description "[The aim of the study was to search for mutations of SCNN1B and SCNN1G in an Italian family with apparently dominant autosomal transmission of a clinical phenotype consistent with Liddle's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP661136.RASGYGr6gajTbgMLLWOedmFfVm1My7E9sm60sdlwoGEfA130_provenance.
- NP29101.RAH9eZUyecXI4lhvApANpFK4UvH7gl1FA_9Xb6lzHkfko130_assertion description "[The aim of the study was to search for mutations of SCNN1B and SCNN1G in an Italian family with apparently dominant autosomal transmission of a clinical phenotype consistent with Liddle's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29101.RAH9eZUyecXI4lhvApANpFK4UvH7gl1FA_9Xb6lzHkfko130_provenance.
- assertion description "[The aim of the study was to search for mutations of SCNN1B and SCNN1G in an Italian family with apparently dominant autosomal transmission of a clinical phenotype consistent with Liddle's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The aim of the study was to search for mutations of SCNN1B and SCNN1G in an Italian family with apparently dominant autosomal transmission of a clinical phenotype consistent with Liddle's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The aim of the study was to search for mutations of SCNN1B and SCNN1G in an Italian family with apparently dominant autosomal transmission of a clinical phenotype consistent with Liddle's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The aim of the study was to search for mutations of SCNN1B and SCNN1G in an Italian family with apparently dominant autosomal transmission of a clinical phenotype consistent with Liddle's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[The aim of the study was to search for mutations of SCNN1B and SCNN1G in an Italian family with apparently dominant autosomal transmission of a clinical phenotype consistent with Liddle's syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.