Point mutations in the lamin A (LMNA) gene cause several human diseases, ranging from congenital muscular dystrophy to premature aging, collectively known as laminopathies, which affect skeletal ...
A groundbreaking study published in this week’s issue of PNAS by scientists from Israel and Ghana shows that an evolutionarily significant mutation in the human APOL1 gene arises not randomly but more ...
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Study links somatic mutations to autoimmune disease development
For decades, the standard explanation for autoimmune diseases like rheumatoid arthritis has rested on two pillars: inherited ...
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