Afficher la couverture 'Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior | Harris, Holly' en grand format
/5

0 avis

Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior

Archive ouverte

Harris, Holly | Nakayama, Tojo | Lai, Jenny | Zhao, Boxun | Argyrou, Nikoleta | Gubbels, Cynthia | Soucy, Aubrie | Genetti, Casie | Suslovitch, Victoria | Rodan, Lance | Tiller, George | Lesca, Gaetan | Gripp, Karen | Asadollahi, Reza | Hamosh, Ada | Applegate, Carolyn | Turnpenny, Peter | Simon, Marleen E.H. | Volker-Touw, Catharina M.L. | Gassen, Koen L.I. Van | Binsbergen, Ellen Van | Pfundt, Rolph | Gardeitchik, Thatjana | Vries, Bert B.A. De | Immken, Ladonna | Buchanan, Catherine | Willing, Marcia | Toler, Tomi | Fassi, Emily | Baker, Laura | Vansenne, Fleur | Wang, Xiadong | Ambrus, Julian | Fannemel, Madeleine | Posey, Jennifer | Agolini, Emanuele | Novelli, Antonio | Rauch, Anita | Boonsawat, Paranchai | Fagerberg, Christina | Larsen, Martin | Kibaek, Maria | Labalme, Audrey | Poisson, Alice | Payne, Katelyn | Walsh, Laurence | Aldinger, Kimberly | Balciuniene, Jorune | Skraban, Cara | Gray, Christopher | Murrell, Jill | Bupp, Caleb | Pascolini, Giulia | Grammatico, Paola | Broly, Martin | Küry, Sébastien | Nizon, Mathilde | Rasool, Iqra Ghulam | Zahoor, Muhammad Yasir | Kraus, Cornelia | Reis, André | Iqbal, Muhammad | Uguen, Kevin | Audebert-Bellanger, Severine | Ferec, Claude | Redon, Sylvia | Baker, Janice | Wu, Yunhong | Zampino, Guiseppe | Syrbe, Steffan | Brosse, Ines | Jamra, Rami Abou | Dobyns, William | Cohen, Lilian | Blomhoff, Anne | Mignot, Cyril | Keren, Boris | Courtin, Thomas | Agrawal, Pankaj | Beggs, Alan | Yu, Timothy

Edité par CCSD ; Nature Publishing Group -

International audience

Consulter en ligne

Suggestions

Du même auteur

Widening of the genetic and clinical spectrum of Lamb–Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency

Archive ouverte | Zawerton, Ash | CCSD

International audience

Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

Archive ouverte | Rodan, Lance | CCSD

International audience. Purpose:CACNA1C encodes the alpha-1-subunit of a voltage-dependent L-type calcium channel expressed in human heart and brain. Heterozygous variants in CACNA1C have previously been reported in...

Clinical and genetic delineation of autosomal recessive and dominant ACTL6B-related developmental brain disorders

Archive ouverte | Cali, Elisa | CCSD

International audience. PurposeThis study aims to comprehensively delineate the phenotypic spectrum of ACTL6B-related disorders, previously associated with both autosomal recessive and autosomal dominant neurodevelo...

Chargement des enrichissements...