Zobrazeno 1 - 2
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pro vyhledávání: '"AH Luo Clayton"'
Autor:
BB Gundersen, WT O’Brien, MD Schaffler, MN Schultz, T Tsukahara, S Martin Lorenzo, V Nalesso, AH Luo Clayton, T Abel, JN Crawley, SR Datta, Y Herault
A microdeletion on human chromosome 16p11.2 is one of the most common copy number variants associated with autism spectrum disorder and other neurodevelopmental disabilities. Arbaclofen, a GABA(B) receptor agonist that is FDA-approved for treating sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51805576f66a8faa2114ede796687f20
https://doi.org/10.1101/2023.05.01.538987
https://doi.org/10.1101/2023.05.01.538987
Autor:
Gundersen BB; Simons Foundation, New York, NY., O'Brien WT; University of Pennsylvania, Philadelphia, PA., Schaffler MD; MIND Institute, University of California Davis School of Medicine, Sacramento, CA., Schultz MN; MIND Institute, University of California Davis School of Medicine, Sacramento, CA., Tsukahara T; Harvard Medical School, Boston, MA., Lorenzo SM; Université de Strasbourg, CNRS UMR7104, INSERM U1258, Institut de Genetique et de Biologie Moleculaire et Cellulaire (IGBMC), Illkirch cedex, France., Nalesso V; Université de Strasbourg, CNRS UMR7104, INSERM U1258, Institut de Genetique et de Biologie Moleculaire et Cellulaire (IGBMC), Illkirch cedex, France., Luo Clayton AH; NIH BRAIN Initiative, Bethesda, MD., Abel T; University of Iowa, Iowa City, IA., Crawley JN; MIND Institute, University of California Davis School of Medicine, Sacramento, CA., Datta SR; Harvard Medical School, Boston, MA., Herault Y; Université de Strasbourg, CNRS UMR7104, INSERM U1258, Institut de Genetique et de Biologie Moleculaire et Cellulaire (IGBMC), Illkirch cedex, France.
Publikováno v:
BioRxiv : the preprint server for biology [bioRxiv] 2023 Sep 14. Date of Electronic Publication: 2023 Sep 14.
