MONDAY, Sept. 16, 2024 -- People with rare genetic variants linked to degenerative brain disorders like Parkinson’s disease are at increased risk of...
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Scientists at deCODE genetics, a subsidiary of AMGEN, have discovered rare sequence variants, predicted to cause a loss of function of ITSN1, that are associated with a high risk of Parkinson's Disease.
MONDAY, Sept. 16, 2024 -- People with rare genetic variants linked to degenerative brain disorders like Parkinson’s disease are at increased risk of...
In a recent study published in Nature Genetics, researchers at the Radcliffe Department of Medicine have discovered a new and more complex way that...
In a recent study published in Nature Genetics, researchers at the Radcliffe Department of Medicine have discovered a new and more complex way that...
A study reveals that common genetic variants in CCDC141 and SCN10A affect Wolff-Parkinson-White syndrome, increasing the risk of life-threatening...
Accessory conduction pathways in the heart, associated with medlinkWolff-Parkinson-White syndrome/medlink, can lead to rhythm disturbances uncovered
A new study from Beth Israel Deaconess Medical Center (BIDMC) has found that people with a history of damage to the lining of their upper...
A new study from Beth Israel Deaconess Medical Center (BIDMC) has found that people with a history of damage to the lining of their upper...
TUESDAY, Sept. 3, 2024 -- Cases of menopause occurring before the age of 40 can be a major cause of distress and discomfort for women, but researchers...
Lipoprotein(a) is a lipid particle and a common genetic cause of cardiovascular diseases. 20% of the world population carries this genetic risk...
WEDNESDAY, Sept. 4, 2024 -- Genetic predisposition to high ferritin and serum iron status is associated with a lower risk for developing rheumatoid...