A bsurprising genetic cause was revealed for a rare inherited blindness disease called medlinkRetinitis Pigmentosa (RP)/medlink that contributes
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Maroc - MEDINDIA.NET - Medindia Health News - 15/Jan 18:11
Discovery of genetic glitches in gene formatting (RNU4-2 mutations) discloses a new cause for blindness, solving retinal cases for scores of families.
A bsurprising genetic cause was revealed for a rare inherited blindness disease called medlinkRetinitis Pigmentosa (RP)/medlink that contributes
A bsurprising genetic cause was revealed for a rare inherited blindness disease called medlinkRetinitis Pigmentosa (RP)/medlink that contributes
Genetic mapping reveals mania drives most inherited risk in bipolar disorder, identifying new gene regions and calcium channel pathways.
A groundbreaking genetic study in Kerala has identified a more aggressive Mpox variant, Clade Ib, linked to international travel and ongoing...
A new single-cell profiling technique has mapped pre-malignant gene mutations and their effects in solid tissues for the first time, in a study led by...
Scientists at University College London have uncovered new evidence suggesting that a single gene, called APOE, may be the key factor behind most...
Scientists at University College London have uncovered new evidence suggesting that a single gene, called APOE, may be the key factor behind most...
Sharp increase in leading cause of irreversible but preventable blindness driven by ageing population and shows need for early diagnosis
New research has revealed that many psychiatric disorders share a common genetic root, a discovery with the potential to transform the diagnosis and...
New research has revealed that many psychiatric disorders share a common genetic root, a discovery with the potential to transform the diagnosis and...