A Novel Homozygous Missense Variant in the LRRC32 Gene Is Associated With a New Syndrome of Cleft Palate, Progressive Vitreoretinopathy, Growth Retardation, and Developmental Delay

Added 45 days ago (17.05.2022)
Authors: Zufit Hexner-Erlichman; Boris Fichtman; Yoav Zehavi; Morad Khayat; Haneen Jabaly-Habib; Lee S. Izhaki-Tavor; Moshe Dessau; Orly Elpeleg; Ronen Spiegel
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