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New SMS mutation leads to a striking reduction in spermine synthase protein function and a severe form of Snyder–Robinson X-linked recessive mental retardation syndrome
  1. Dr A Laurato Sertié, Rua do Matão 277, Depto. Genética e Biologia Evolutiva, Instituto de Biociências, USP, São Paulo, SP, 05508-900, Brazil; asertie{at}hotmail.com
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Citation

de Alencastro G, McCloskey DE, Kliemann SE, et al
New SMS mutation leads to a striking reduction in spermine synthase protein function and a severe form of Snyder–Robinson X-linked recessive mental retardation syndrome

Publication history

  • Received December 6, 2007
  • Revised May 2, 2008
  • Accepted May 12, 2008
  • First published June 11, 2008.
Online issue publication 
April 27, 2016

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