Thursday, November 19, 2020

CLCN6 identified as disease gene for a severe form of lysosomal neurodegenerative disease

A mutation in the CLCN6 gene is associated with a novel, particularly severe neurodegenerative disorder. Scientists have now analyzed the effect of a point mutation that was found in three unrelated affected children.

from Top Health News -- ScienceDaily https://ift.tt/2IXCELO

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Study finds untreated sleep apnea doubles Parkinson’s risk

A massive veteran study found a strong connection between untreated sleep apnea and a higher chance of Parkinson’s. CPAP users had much lowe...