Paper

Tree Display

AceDB Schema

XML Display

Feedback

Paper Report for: Nakanishi_2017_PLoS.Genet_13_e1006940

Reference
Title: Functional significance of rare neuroligin 1 variants found in autism
Nakanishi M, Nomura J, Ji X, Tamada K, Arai T, Takahashi E, Bucan M, Takumi T
Ref: PLoS Genet, 13:e1006940, 2017 : PubMed

        


Related information
Gene_Locus : human-NLGN1
Mutation : H795Y_human-NLGN1, P89L_human-NLGN1, T90I_human-NLGN1, L269P_human-NLGN1, G297E_human-NLGN1,

Citations formats
Nakanishi M, Nomura J, Ji X, Tamada K, Arai T, Takahashi E, Bucan M, Takumi T (2017)
Functional significance of rare neuroligin 1 variants found in autism
PLoS Genet 13: e1006940

Nakanishi M, Nomura J, Ji X, Tamada K, Arai T, Takahashi E, Bucan M, Takumi T (2017)
PLoS Genet 13: e1006940


Send your questions or comments to :
Mail to: Nicolas Lenfant, Thierry Hotelier, Yves Bourne, Pascale Marchot and Arnaud Chatonnet.
Please cite: Lenfant 2013 Nucleic.Acids.Res. or Marchot Chatonnet 2012 Prot.Pept Lett.
For technical information about these pages see:
ESTHER Home Page and ACEDB Home Page
AcePerl Lincoln Stein Home Page
webmaster

Acknowledgements and disclaimer