Matches in Nanopublications for { ?s ?p "[Also, AD and PD clinical diagnoses in patients who carry PGRN null mutations likely result from etiologic heterogeneity rather than PGRN haploinsufficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 1 of
1
with 100 items per page.
- NP755631.RAiHfPPsBv95M5Yd3yGAQ36-8gHvGVOOJgqO2wCpIJHvg130_assertion description "[Also, AD and PD clinical diagnoses in patients who carry PGRN null mutations likely result from etiologic heterogeneity rather than PGRN haploinsufficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755631.RAiHfPPsBv95M5Yd3yGAQ36-8gHvGVOOJgqO2wCpIJHvg130_provenance.