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  Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes.

Endele, S., Rosenberger, G., Geider, K., Popp, B., Tamer, C., Stefanova, I., et al. (2010). Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes. Nature Genetics., 42(11), 1021-1026. doi:10.1038/ng.677.

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Genre: Journal Article
Alternative Title : Nat. Genet.

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 Creators:
Endele, Sabine, Author
Rosenberger, Georg, Author
Geider, Kirsten, Author
Popp, Bernt, Author
Tamer, Ceyhun, Author
Stefanova, Irina, Author
Milh, Mathieu, Author
Kortüm, Fanny, Author
Fritsch, Angela, Author
Pientka, Friederike K, Author
Hellenbroich, Yorck, Author
Kalscheuer, Vera M1, Author
Kohlhase, Jürgen, Author
Moog, Ute, Author
Rappold, Gudrun, Author
Rauch, Anita, Author
Ropers, Hans-Hilger2, Author           
von Spiczak, Sarah, Author
Tönnies, Holger, Author
Villeneuve, Nathalie, Author
Villard, Laurent, AuthorZabel, Bernhard, AuthorZenker, Martin, AuthorLaube, Bodo, AuthorReis, André, AuthorWieczorek, Dagmar, AuthorVan Maldergem, Lionel, AuthorKutsche, Kerstin, Author more..
Affiliations:
1Max Planck Society, ou_persistent13              
2Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society, ou_1433549              

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Language(s): eng - English
 Dates: 2010-10-03
 Publication Status: Issued
 Pages: -
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Title: Nature Genetics.
  Alternative Title : Nat. Genet.
Source Genre: Journal
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Pages: - Volume / Issue: 42 (11) Sequence Number: - Start / End Page: 1021 - 1026 Identifier: ISSN: 1061-4036