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Plasma levels of activated protein C in healthy subjects and patients with previous venous thromboembolism: Relationships with plasma homocysteine levels
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In cases of familial late-onset PD, 8.67% exhibited mutations in GBA (heterozygous), HTRA2, and SNCA, while 30.03% had disease-causing genes in CHCHD2, DJ-1, GBA (heterozygous), LRRK2, PINK1, and PRKN (Sun et al., 2023)
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