Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleA novel homozygous <italic>AP4B1</italic> mutation in two brothers with AP‐4 deficiency syndrome and ocular anomalies.AuthorsAccogli, Andrea; Hamdan, Fadi F.; Poulin, Chantal; Nassif, Christina; Rouleau, Guy A.; Michaud, Jacques L.; Srour, MyriamPublicationAmerican Journal of Medical Genetics. Part A, 2018, Vol 176, Issue 4, p985ISSN1552-4825Publication typeArticleDOI10.1002/ajmg.a.38628