Matches in Nanopublications for { ?s ?p "[Mutations in the polyglutamine tract binding protein 1 gene (PQBP1) have recently been reported in four XLMR disorders (Renpenning, Hamel cerebro-palato-cardiac, Sutherland-Haan, and Porteous syndromes) as well as in several other families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- assertion description "[Mutations in the polyglutamine tract binding protein 1 gene (PQBP1) have recently been reported in four XLMR disorders (Renpenning, Hamel cerebro-palato-cardiac, Sutherland-Haan, and Porteous syndromes) as well as in several other families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP836302.RAuOOLRrw8oR9cPfkITP6Kpi00vU9TS49lCXGwCxfPuzw130_assertion description "[Mutations in the polyglutamine tract binding protein 1 gene (PQBP1) have recently been reported in four XLMR disorders (Renpenning, Hamel cerebro-palato-cardiac, Sutherland-Haan, and Porteous syndromes) as well as in several other families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP836302.RAuOOLRrw8oR9cPfkITP6Kpi00vU9TS49lCXGwCxfPuzw130_provenance.
- NP552615.RA5SoZjjN4J415rPoMcdMpGroa1KvbtEqj3N6BBcJVtH0130_assertion description "[Mutations in the polyglutamine tract binding protein 1 gene (PQBP1) have recently been reported in four XLMR disorders (Renpenning, Hamel cerebro-palato-cardiac, Sutherland-Haan, and Porteous syndromes) as well as in several other families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP552615.RA5SoZjjN4J415rPoMcdMpGroa1KvbtEqj3N6BBcJVtH0130_provenance.