Deletion of MAOA and MAOB in a male patient causes severe developmental delay, intermittent hypotonia and stereotypical hand movements-Reference-Cited by-同舟云学术

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Deletion of MAOA and MAOB in a male patient causes severe developmental delay, intermittent hypotonia and stereotypical hand movements

Published:2010-05-19 Issue:10 Volume:18 Page:1095-1099
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Whibley Annabel,Urquhart Jill,Dore Jonathan,Willatt Lionel,Parkin Georgina,Gaunt Lorraine,Black Graeme,Donnai Dian,Raymond F Lucy

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/ejhg201041.pdf

Reference29 articles.

1. Shih JC, Thompson RF : Monoamine oxidase in neuropsychiatry and behavior. Am J Hum Genet 1999; 65: 593–598.

2. Bortolato M, Chen K, Shih JC : Monoamine oxidase inactivation: from pathophysiology to therapeutics. Adv Drug Deliv Rev 2008; 60: 1527–1533.

3. Chen ZY, Denney RM, Breakefield XO : Norrie disease and MAO genes: nearest neighbors. Hum Mol Genet 1995; 4: 1729–1737.

4. Lan NC, Heinzmann C, Gal A et al: Human monoamine oxidase A and B genes map to Xp 11.23 and are deleted in a patient with Norrie disease. Genomics 1989; 4: 552–559.

5. Nicotra A, Pierucci F, Parvez H, Senatori O : Monoamine oxidase expression during development and aging. Neurotoxicology 2004; 25: 155–165.

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