Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome.
Bi W; Saifi GM; Shaw CJ; Walz K; Fonseca P; Wilson M; Potocki L; Lupski JR; Human Genetics, 2004, vol. 115, issue 6, p 515, ISSN 03406717. ISBN 03406717.

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