Potential drug target found for treating rare genetic disorder in children
February 2, 20214 min read716 words
Published: February 2, 2021  |  4 min read716 words
Scientists have identified a potential new treatment approach for Hutchinson-Gilford progeria syndrome (HGPS), a progressive genetic disorder that causes rapid and premature aging in children.The findings in mice, published today in eLife, show that blocking a protein called ICMT...
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