PubMed: Intrafamilial Phenotypic Variability in the C9orf72 Gene Expansion: 2 Case Studies. https://t.co/nbKPUNPEjn
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RT @BrainMind_Usyd: #Research highlights variability in disease onset and disease course in patients with C9orf72 genetic mutation #MND #FT…
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#Research highlights variability in disease onset and disease course in patients with C9orf72 genetic mutation #MND #FTD #USydBMC https://t.co/qOm1hgx2O5
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Excellent new paper reveals that knowing that there is a genetic risk of dementia (C9orf72 mutation) doesn’t necessarily predict the progression of the disease and this needs to be conveyed to at-risk families during counselling.