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Comment
. 2006 Mar 1;140(5):419-20.
doi: 10.1002/ajmg.a.31046.

AGTR2 in brain development and function

Virginie S Vervoort  1 , Greagory Guzauskas, John Archie, Charles E Schwartz, Roger E Stevenson, Anand K Srivastava
Affiliations
Comment

AGTR2 in brain development and function

Virginie S Vervoort et al. Am J Med Genet A. .
No abstract available

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References

    1. Bienvenu T, Poirier K, Van Esch H, Hamel B, Moraine C, Fryns JP, Ropers HH, Beldjord C, Yntema HG, Chelly J. Rare polymorphic variants of the AGTR2 gene in boys with nonspecific mental retardation. J Med Genet. 2003;40:357–359. - PMC - PubMed
    1. Chelly J, Mandel JL. Monogenic causes of X-linked mental retardation. Nat Rev Genet. 2001;2:669–680. - PubMed
    1. Erdmann J, Dahmlow S, Guse M, Hetzer R, Regitz-Zagrosek V. The assertion that a G21V mutation in AGTR2 causes mental retardation is not supported by other studies. Hum Genet. 2004;114:396. - PubMed
    1. Herbst DS, Miller JR. Nonspecific X-linked mental retardation II: The frequency in British Columbia. Am J Med Genet. 1980;7:461–469. - PubMed
    1. Huang D, Sun W, Strom CM. Sequence variations in AGTR2 are unlikely to be associated with X-linked mental retardation. Am J Med Genet Part A. 2005;139A:243–244. - PubMed

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