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Variant in the synaptonemal complex protein S

<p>Scientists a<strong>t deCODE genetics</strong>, a subsidiary of <strong>Amgen</strong> and their collaborators from Iceland, Denmark and USA publish a new study today in <strong>Nature Structural and Molecular Biology </strong>that reveals a low- frequency missense variant in the <em>SYCE2</em> gene that increases the risk of pregnancy loss by 22%. In a previous report by deCODE scientists this missense ...
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SYCE2 Genetic Variant Linked to 22% Higher Miscarriage Risk

A significant study identifies a genetic variant in the SYCE2 gene that heightens the risk of miscarriage by 22%, shedding light on the genetic causes of pregnancy loss. Scientists at deCODE genetics, a subsidiary of Amgen and their collaborators from Iceland, Denmark, and the USA published a stu
United States United Kingdom Valgerdur Steinthorsdottir Kari Stefansson Woman Hospital Miscarriage Research Sad Woman Hospital Miscarriage

Gene variant linked to increased miscarriage risk through disrupted chromosome pairing

Scientists at deCODE genetics, a subsidiary of Amgen and their collaborators from Iceland, Denmark and USA published a study today in Nature Structural and Molecular Biology titled "Variant in the synaptonemal complex protein SYCE2 associates with pregnancy loss through effects on recombination".
United States United Kingdom Nature Structural Molecular Biology Molecular Biology

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