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One or more keywords matched the following properties of A 15q13.3 homozygous microdeletion associated with a severe neurodevelopmental disorder suggests putative functions of the TRPM1, CHRNA7, and other homozygously deleted genes.

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has major subject area list Chromosome Deletion; Chromosomes, Human, Pair 15; Developmental Disabilities; Homozygote; Receptors, Nicotinic; TRPM Cation Channels

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  • Developmental Delay Disorder