Matches in Nanopublications for { ?s ?p "[Recessively inherited deletions/duplications and point mutations in the parkin gene are the most common cause of early-onset parkinsonism known so far, but in an increasing number of studies, genetic variations in the serine/threonine kinase domain of the PINK1 gene are found to explain early-onset parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- NP664756.RAeAl_G-hIKiHZHMU5vBRcThrlItD-4kN5-NZd6pSTwus130_assertion description "[Recessively inherited deletions/duplications and point mutations in the parkin gene are the most common cause of early-onset parkinsonism known so far, but in an increasing number of studies, genetic variations in the serine/threonine kinase domain of the PINK1 gene are found to explain early-onset parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP664756.RAeAl_G-hIKiHZHMU5vBRcThrlItD-4kN5-NZd6pSTwus130_provenance.
- assertion description "[Recessively inherited deletions/duplications and point mutations in the parkin gene are the most common cause of early-onset parkinsonism known so far, but in an increasing number of studies, genetic variations in the serine/threonine kinase domain of the PINK1 gene are found to explain early-onset parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP709614.RABdyg_yaG3kue3Yvt9nnkJ0yTwKEFpcyCYKGlUAixl6g130_assertion description "[Recessively inherited deletions/duplications and point mutations in the parkin gene are the most common cause of early-onset parkinsonism known so far, but in an increasing number of studies, genetic variations in the serine/threonine kinase domain of the PINK1 gene are found to explain early-onset parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709614.RABdyg_yaG3kue3Yvt9nnkJ0yTwKEFpcyCYKGlUAixl6g130_provenance.
- NP709616.RAuj8vOP3ECTJxRuhx8dzWqAqh-AECzxBmxJSDFyRcRLc130_assertion description "[Recessively inherited deletions/duplications and point mutations in the parkin gene are the most common cause of early-onset parkinsonism known so far, but in an increasing number of studies, genetic variations in the serine/threonine kinase domain of the PINK1 gene are found to explain early-onset parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709616.RAuj8vOP3ECTJxRuhx8dzWqAqh-AECzxBmxJSDFyRcRLc130_provenance.
- NP374100.RAxjRx7X1TX831JbrymKS9PvlYnHA15KVh53uhVpp8FSs130_assertion description "[Recessively inherited deletions/duplications and point mutations in the parkin gene are the most common cause of early-onset parkinsonism known so far, but in an increasing number of studies, genetic variations in the serine/threonine kinase domain of the PINK1 gene are found to explain early-onset parkinsonism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374100.RAxjRx7X1TX831JbrymKS9PvlYnHA15KVh53uhVpp8FSs130_provenance.