Abnormal circadian rhythm of melatonin in Smith-Magenis syndrome patients with RAI1 point mutations
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.34098/fullpdf
Reference34 articles.
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2. RAI1 point mutations, CAG repeat variation, and SNP analysis in non-deletion Smith-Magenis syndrome;Bi;Am J Med Genet Part A,2006
3. Mutations of RAI1, a PHD-containing protein, in nondeletion patients with Smith-Magenis syndrome;Bi;Hum Genet,2004
4. Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouse;Bi;Genome Res,2002
5. Melatonin in humans;Brzezinski;N Engl J Med,1997
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