A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome-Reference-Cited by-同舟云学术

A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndrome

Published:2007-03-04 Issue:4 Volume:39 Page:451-453
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Risheg Hiba,Graham John M,Clark Robin D,Rogers R Curtis,Opitz John M,Moeschler John B,Peiffer Andreas P,May Melanie,Joseph Sumy M,Jones Julie R,Stevenson Roger E,Schwartz Charles E,Friez Michael J

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1992.pdf

Reference15 articles.

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3. Philibert, R.A. et al. Mol. Psychiatry 3, 303–309 (1998).

4. Friez, M.J. et al. Hum. Genet. 106, 36–39 (2000).

5. Beyer, K.S. et al. Am. J. Med. Genet. 114, 110–115 (2002).

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