Inactivation of Rai1 in mice recapitulates phenotypes observed in chromosome engineered mouse models for Smith–Magenis syndrome

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Human Molecular Genetics, Vol. 14, Iss. 8, 2005-04 ,pp. : 983-995

Oxford University Press

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Behavioral characterization of mouse models for Smith–Magenis syndrome and dup(17)(p11.2p11.2)

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Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome

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Identification of Nine New RAI1-Truncating Mutations in Smith-Magenis Syndrome Patients without 17p11.2 Deletions

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Biochemical, phenotypic and neurophysiological characterization of a genetic mouse model of RSH/Smith–Lemli–Opitz syndrome

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