NTNG1mutations are a rare cause of Rett syndrome-Reference-Cited by-同舟云学术

NTNG1mutations are a rare cause of Rett syndrome

Published:2006-04-01 Issue:7 Volume:140A Page:691-694
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Archer Hayley L.,Evans Julie C.,Millar David S.,Thompson Peter W.,Kerr Alison M.,Leonard Helen,Christodoulou John,Ravine David,Lazarou Lazarus,Grove Lucy,Verity Christopher,Whatley Sharon D.,Pilz Daniela T.,Sampson Julian R.,Clarke Angus J.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference35 articles.

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3. Altered development of glutamate and GABA receptors in the basal ganglia of girls with Rett syndrome;Blue;Exp Neurol,1999

4. Disruption of Netrin G1 by a balanced chromosome translocation in a girl with Rett syndrome;Borg;Eur J Hum Genet,2005

5. ESEfinder: A web resource to identify exonic splicing enhancers;Cartegni;Nucl Acid Res,2003

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