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Childhood deafness: Researchers identify over 200 mutations, including previously unknown variants
Deafness, the most common sensorineural hearing loss at all stages of life, occurs either independently or as part of ...
Nearly 1 in 7 adults in the United States lives with chronic kidney disease, a condition that often advances quietly until ...
A newly identified and rare genetic variant slows the growth of mutated blood stem cells and reduces the risk of leukemia.
ScienceAlert on MSN
This rare genetic mutation kills brain cells, and we finally know why
Experiments on an ultra-rare genetic mutation that causes neurodegeneration in children have helped uncover a new mechanism by which brain cells die. The findings raise the possibility that similar ...
Mitochondria are well known as the powerhouses of the cell because of their energy generating capabilities. These little organelles are very special, because they also carry their own tiny little ...
The prothrombin gene mutation increases your risk of severe blood clots. Medications, regular checkups, and healthy lifestyle habits can help reduce this risk. The prothrombin gene plays a crucial ...
This report is based on a recent in-depth article by the BBC, which examined how modern genetics is transforming scientific understanding of autism and reigniting debates within the autistic community ...
A rare genetic variant found in families affected by schizophrenia completely abolishes the function of TAAR1, an emerging ...
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