Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
Julia Vornweg, Sven Gläser, M. Ahmad‐Anwar, Andreas Zimmer, Marius Kuhn, Steffen Hörer, Georg Christoph Korenke, Julia Grothaus, Hagen Ott, Judith Fischer
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