GRIN2A c.1007+6501C>T

Variant ID: 16-10025315-G-A

NM_001134407.1(GRIN2A):c.1007+6501C>T

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Abnormal melatonin synthesis in autism spectrum disorders.

Molecular Psychiatry
Melke, J J; Goubran Botros, H H; Chaste, P P; Betancur, C C; Nygren, G G; Anckarsäter, H H; Rastam, M M; Ståhlberg, O O; Gillberg, I C IC; Delorme, R R; Chabane, N N; Mouren-Simeoni, M-C MC; Fauchereau, F F; Durand, C M CM; Chevalier, F F; Drouot, X X; Collet, C C; Launay, J-M JM; Leboyer, M M; Gillberg, C C; Bourgeron, T T
Publication Date: 2008-01

Variant appearance in text: rs4782053
PubMed Link: 17505466
Variant Present in the following documents:
  • Main text
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