Martin Zenker, Corinne Antignac, Friedhelm Hildebrandt and colleagues report that mutations in OSGEP, TP53RK, TPRKB and LAGE3, genes encoding KEOPS-complex subunits, cause Galloway–Mowat ...

Kansas Parents of 2 Girls With Microcephaly Share Joys, Struggles of Family Life Scott and Gwen Hartley have two daughters with the same neurological condition and they share their milestones online.