Learn how researchers cracked a genetic mystery, diagnosing undiagnosed diseases by identifying FLVCR1 mutations.
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Researchers used DRIVE to uncover undiagnosed Long QT syndrome carriers by analyzing shared genomic segments and identical-by-descent variants.
Learn how researchers cracked a genetic mystery, diagnosing undiagnosed diseases by identifying FLVCR1 mutations.
Researchers utilised specialised genomic technology at the University of Calgary, Canada, to enhance our understanding of Marjolin’s ulcer (MU), a...
TUESDAY, Nov. 12, 2024 -- A cutting-edge genetic test can rapidly detect and identify almost any kind of disease-causing microorganism in the human...
An international team of researchers has provided a genetic diagnosis for 30 individuals whose condition was undiagnosed for years despite extensive...
Researchers have identified an FDA-approved drug that could offer new hope for patients with the rare, fatal genetic disorders Sandhoff and...
Avidity Biosciences expands its pipeline to include two new drugs targeting rare genetic cardiomyopathies.
Avidity Biosciences expands its pipeline to include two new drugs targeting rare genetic cardiomyopathies.
A recent study by scientists at deCODE genetics, published in Nature Communications, offers new insights into how body mass index (BMI) can influence...
NEW YORK--(BUSINESS WIRE)--Nov. 11, 2024-- Neurogene Inc. (Nasdaq: NGNE), a clinical-stage company founded to bring life-changing genetic medicines to...
Variants of the PER3 gene disrupt adrenal adaptation to winter light, leading to serotonin disruption and depression-like behaviors in humanized mice...