Associated Papers
Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defects.
Rujano MA et al.
The Journal of Experimental Medicine, 2017
Characterization of Disease-Associated Mutations in Human Transmembrane Proteins.
Molnár J et al.
Plos One, 2016
26986070 (PubMed )
Supplement: pone.0151760.s001.xlsx › polymorphism
Association of (pro)renin receptor gene polymorphisms with lacunar infarction and left ventricular hypertrophy in Japanese women: the Ohasama study.
Hirose T et al.
Hypertension Research : Official Journal of the Japanese Society of Hypertension, 2011
Association of (pro)renin receptor gene polymorphism with blood pressure in Japanese men: the Ohasama study.
Hirose T et al.
American Journal of Hypertension, 2009
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