MAOA/B deletion syndrome in male siblings with severe developmental delay and sudden loss of muscle tonus-Reference-Cited by-同舟云学术

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MAOA/B deletion syndrome in male siblings with severe developmental delay and sudden loss of muscle tonus

Published:2014-01 Issue:1 Volume:36 Page:64-69
ISSN:0387-7604
Container-title:Brain and Development
language:en
Short-container-title:Brain and Development

Author:

Saito Mari,Yamagata Takanori,Matsumoto Ayumi,Shiba Yusuke,Nagashima Masako,Taniguchi Shuhei,Jimbo Eriko,Momoi Mariko Y

Publisher

Elsevier BV

Subject

Neurology (clinical),Developmental Neuroscience,General Medicine,Pediatrics, Perinatology and Child Health

Reference10 articles.

1. Monoamine oxidase: from genes to behavior;Shih;Ann Rev Neurosci,1999

2. Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A;Brunner;Science,1993

3. 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

4. Marked amine and amine metabolite changes in Norrie disease patients with an X-chromosomal deletion affecting monoamine oxidase;Murphy;J Neurochem,1990

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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