SOBP Is Mutated in Syndromic and Nonsyndromic Intellectual Disability and Is Highly Expressed in the Brain Limbic System
Year: 2010
Type: article
Authors: Efrat Birk, Adi Har-Zahav, Chiara M. Manzini, Metsada Pasmanik-Chor, Liora Kornreich, Christopher A. Walsh, Konrad Noben-Trauth, Adi Albin, Amos J. Simon, Laurence Colleaux, Yair Morad, Limor Rainshtein, David J. Tischfield, Peter Wang, Nurit Magal, Idit Maya, Noa Shoshani, Gideon Rechavi, Doron Gothelf, Gal Maydan, Mordechai Shohat, Lina Basel-Vanagaite
Institutions: Tel Aviv University, Boston Children's Hospital, Manton Center for Orphan Disease Research, Schneider Children's Medical Center, National Institutes of Health, National Institute on Deafness and Other Communication Disorders, Rabin Medical Center, Sheba Medical Center, Hôpital Necker-Enfants Malades, Inserm, Université Paris Descartes, Assaf Harofeh Medical Center, Edmond and Lily Safra Children's Hospital
Language: English
Subfield: Genetics
Domain: Life Sciences
Open Access status: bronze
OpenAlex ID: W2147159231