De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: A genomics approach to personalized medicine-Reference-Cited by-同舟云学术

De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: A genomics approach to personalized medicine

Published:2012-05 Issue:5 Volume:55 Page:349-353
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

O’Leary Ryan E.,Shih Jean C.,Hyland Keith,Kramer Nancy,Asher Y. Jane Tavyev,Graham John M.

Funder

Steven Spielberg Pediatric Research Center

NIH/NICHD

Medical Genetics NIH/NIGMS

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference23 articles.

1. Monoamine oxidase: basic and clinical aspects;Yasuhara;VPS, Zeist, Netherland,1993

2. Monoamine oxidases regulate telencephalic neural progenitors in late embryonic and early postnatal development;Cheng;J. Neurosci.,2010

3. Monoamine oxidase: from genes to behavior;Shih;Annu. Rev. Neurosci.,1999

4. Specific genetic deficiencies of the A and B isoenzymes of monoamine oxidase are characterized by distinct neurochemical and clinical phenotypes;Lenders;J. Clin. Invest.,1996

5. Clinical, biochemical, and neuropsychiatric evaluation of a patient with a contiguous gene syndrome due to a microdeletion Xp11.3 including the Norrie disease locus and monoamine oxidase (MAOA and MAOB) genes;Collins;Am. J. Med. Genet.,1992

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