Novel COL6A1 Gene Variant Linked to Rare Muscle Disorder in Child
A novel homozygous COL6A1 variant classified as uncertain has been linked to classic Ullrich congenital muscular dystrophy in a three-year-old ...
Tag: congenital hypotonia
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Mothers who receive childcare support from maternal grandparents show more parental warmth, finds NTU Singapore study
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University of Seville Breaks 120-Year-Old Mystery, Revises a Key Einstein Concept
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Bee body mass, pathogens and local climate influence heat tolerance
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Researchers record first-ever images and data of a shark experiencing a boat strike
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Groundbreaking Clinical Trial Reveals Lubiprostone Enhances Kidney Function
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