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NTNG1 mutations are a rare cause of Rett syndrome

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

Publisher: John Wiley and Sons
Year: 2006
Tongue: English
Weight: 86 KB
Volume: 140A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.31133

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