The headline is broadly defensible, but the qualifications matter. Effect sizes vary by population, the strongest claims rest on shorter trials, and credible voices push back on how it's typically framed.
prader-willi is a genetic disorder in which rather than having a single gene affected there is a region of the which is in most instances not all but the majority of instances deleted so there's a region of chromosome 15 in which there is a large deletion that is a region that has normally 20 or so genes in it and when deleted when the paternal the father's copy of this interval is deleted the individual becomes has a very characteristic phenotype
Every Sunday: the week’s new conflicts and verdict changes — and nothing else.
Native comments, Twitter mentions, and Reddit threads about this claim — surfaced together so the conversation isn't fragmented across platforms.
Bookmarking — the dossier-vs-overview split is the right call. Most of the time I want overview; sometimes I want receipts.
Would love a "what would change this verdict" RSS feed. Sign me up if it exists.