New insights into Brunner syndrome and potential for targeted therapy-Reference-Cited by-同舟云学术

New insights into Brunner syndrome and potential for targeted therapy

Published:2015-04-19 Issue:1 Volume:89 Page:120-127
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Palmer E.E.¹²,Leffler M.¹,Rogers C.¹,Shaw M.³,Carroll R.³,Earl J.⁴⁵,Cheung N.W.⁴⁶,Champion B.⁴⁶,Hu H.⁷,Haas S.A.⁸,Kalscheuer V.M.⁷,Gecz J.³,Field M.¹

Affiliation:

1. Department of Clinical Genetics; GOLD (Genetics of Learning Disability) service; Waratah New South Wales Australia

2. University of New South Wales; Waratah New South Wales Australia

3. School of Paediatrics and Reproductive Health and Robinson Institute; The University of Adelaide; Adelaide South Australia Australia

4. Department of Paediatrics and Child Health; University of Sydney; Sydney New South Wales Australia

5. Department of Biochemistry; The Children's Hospital at Westmead; Sydney New South Wales Australia

6. Department of Endocrinology; Nepean Hospital; Sydney New South Wales Australia

7. Department of Human Molecular Genetics

8. Department of Computational Molecular Biology; Max Planck Institute for Molecular Genetics; Berlin Germany

Funder

National Health and Medical Research Council

Senior Research Fellowship

EU FP7 project GENCODYS

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/cge.12589/fullpdf

Reference18 articles.

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

3. MAOA-environment interactions: results may vary;Goldman;Biol Psychiatry,2014

4. MAOA deficiency and abnormal behaviour: perspectives on an association;Brunner;Ciba Found Symp,1996

5. Screen for MAOA mutations in target human groups;Schuback;Am J Med Genet,1999

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