Yang, Q., Yang, Q., Zhang, Q., Zhang, Q., Zhou, X., Zhou, X., . . . Luo, J. Whole-exome sequencing identified a novel heterozygous variant in UBAP2L in a Chinese family with neurodevelopmental disorder characterized by impaired language, behavioral abnormalities, and dysmorphic facies. Frontiers Media S.A.
Chicago Style (17th ed.) CitationYang, Qi, et al. Whole-exome Sequencing Identified a Novel Heterozygous Variant in UBAP2L in a Chinese Family with Neurodevelopmental Disorder Characterized by Impaired Language, Behavioral Abnormalities, and Dysmorphic Facies. Frontiers Media S.A.
MLA (9th ed.) CitationYang, Qi, et al. Whole-exome Sequencing Identified a Novel Heterozygous Variant in UBAP2L in a Chinese Family with Neurodevelopmental Disorder Characterized by Impaired Language, Behavioral Abnormalities, and Dysmorphic Facies. Frontiers Media S.A.