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Die autosomal-dominant vererbte Albright-Osteodystrophie (AHO) ist charakterisiert durch einen Symptomenkomplex bestehend aus Minderwuchs, Brachymetakarpie, Fettleibigkeit, rundem Gesicht, kutanen Osteomen und einer mentalen Retardierung. Zu Grunde liegen Mutationen im GNAS-Gen auf Chromosom 20, das für das Gsα-Protein kodiert. Da dieses für die Signaltransduktion verschiedener Peptidhormone verantwortlich...
Set the date range to filter the displayed results. You can set a starting date, ending date or both. You can enter the dates manually or choose them from the calendar.