. . . . . . . "[For those with baseline LV dysfunction, being homozygous for Arg at amino acid position 389 in ?1-AR was associated with decreases in ESV (-46�mL, CI -3.1, -88) and EDV (-40�mL, CI -1.1, -79) and an increase in LVEF (11%, CI 0.3, 22).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:10:18+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .